Birch-TypeReactions Sarpong
Birch-TypeReactions Sarpong
Birch-TypeReactions Sarpong
Birch-Type Reactions
Note: Birch-Type reactions involve the use of water reactive materials, flammables, and toxic gas. It is
performed at cold temperature and, when complete and warms up, generates a substantial amount of
heat.
Moreover, the scale at which this reaction is performed is rather large.
This reaction can NOT be left unattended or performed alone.
It is paramount that researchers be aware of the hazards associated with Birch-Type reactions.
Areas with blue text indicate that information must be provided or modified by researcher prior to
the SOP approval.
This SOP is not a substitute for hands-on training.
Print a copy and insert into your laboratory SOP binder.
Department: Chemistry
Date SOP was written:
1. Purpose
This SOP covers the precautions and safe handling procedures for Birch-type reactions.
Birch-type reactions involve, among other chemicals, water reactive materials (WR) such as, but not
restrictive to, sodium, potassium and lithium, and toxic gas such as ammonia. Those chemicals are
covered by their specific class SOPs.
Before setting-up a Birch-Type reaction, researchers must have read and sign the specific class SOPs of
any chemical involved in this reaction.
If you have questions concerning the applicability of any recommendation or requirement listed in this
procedure, contact the Principal Investigator/Laboratory Supervisor or the campus Chemical Hygiene
Officer at [email protected].
3. Potential Hazards/Toxicity
When running Birch-type reactions, the hazards of the mixture must be considered and procedures for
safe handling and quenching must reflect the hazard properties of each component.
As a reminder, the Globally Harmonized System of Classification and Labeling of Chemicals (GHS) defines
water reactive materials as “substances and mixtures which, in contact with water, emit flammable
gases” and are designated by one or more of the following H codes and hazard statements:
H260 In contact with water releases flammable gases which may ignite spontaneously
H261 In contact with water releases flammable gases
GHS designates ammonia gas (NH3 (g)) by the following H codes and hazard statements:
H221 Flammable gas
H280 Contains gas under pressure; may explode if heated
H314 Causes severe skin burns and eye damage
H331 Toxic if inhaled
H410 Very toxic to aquatic life with long lasting effects
4. Engineering Controls
The following is the set of engineering controls required when running Birch-type reactions:
• Have a sign such as “Ammonia in Use” posted on lab doors.
• Use a clean fume hood, preferably with the sliding sash windows. Keep the sash as low as possible at
all times. Stand behind the sliding windows and reach around to perform the manipulations
required.
• Remove any flammables (squirt bottles, solvents, oil bath) and combustibles (KimWipes, paper
towel) from working area.
• All cylinders and gas cabinets must be clearly labeled with content and hazard information.
• The gas cylinder of ammonia must be placed in a fume hood and anchored using at least one chain
before dispensing the reagent.
• All regulators, valves, and lines must be chemically compatible with ammonia (i.e. Tygon).
Regulators shall be compatible with the size and type of gas cylinder being used and rated for full
cylinder pressure.
• When evaporating ammonia, work under a continuous flow of inert gas (e.g. argon, nitrogen).
• Whenever quenching be sure that it is not done in a sealed vessel as pressure will build up.
Rinse thoroughly with plenty of water using an eyewash station for at least 15 minutes, occasionally
lifting the upper and lower eyelids. Remove contact lenses if possible.
If swallowed
Do NOT induce vomiting unless directed otherwise by the SDS. Never give anything by mouth to an
unconscious person. Rinse mouth with water.
If inhaled
Move into fresh air.
Needle stick/puncture exposure
Wash the affected area with antiseptic soap and warm water for 15 minutes. For mucous membrane
exposure such as eyes, mouth and/or nose, flush the affected area for 15 minutes using an eyewash
station.
• Keep others from entering contaminated area (e.g., use caution tape, barriers, etc.).
• Report the spill to 510-642-3073.
Fire Response
• Call 911 (from a cell phone: 510-642-3333) for assistance with all fires, even if extinguished.
• If the spill ignites, and if you are trained and you feel comfortable to do so, consider extinguishing
the fire with an appropriate fire extinguisher. Use only dry chemical fire extinguishers (classes ABC
or D).
• A can of Met-L-X or dry sand in the work area, within arm’s reach, might be helpful to extinguish any
small fire as it can smother the flames.
• Do not use water to extinguish a WR chemical fire as it may enhance the intensity of the fire. An
exception to this would be in the case of skin contact or ignited clothing/skin. In these cases rinsing
any unreacted chemical off is of primary importance.
• Before using NH3(g) be sure you are in compliance with the University of Berkeley Toxic Gas Program requirements. If you have
questions about Toxic Gas Program requirements, contact EH&S at 642-3073.
• All regulators, valves, and lines must be chemically compatible with the NH3(g). Regulators shall be compatible with the size and
type of gas cylinder being used and rated for full cylinder pressure.
• Know the location of the nearest fire extinguisher, eyewash, and safety shower before beginning work. Have a small beaker or can
of Met-L-X or DRY sand in the work area, within arm’s reach.
• Solvents must be dry.
• Glassware must be dry before using. Either “flame” dry or dry in an oven overnight at a minimum temperature of 120◦C.
• Remove all other flammable materials from the hood to reduce the hazard in case of a fire. Others in the lab must know that you
will be running a Birch-type reaction.
NOTE: Larger quantities (see Scale column below) of WR chemicals can be disposed of as hazardous waste.
• Carefully package and label the wastes with current HWP labels.
• Request waste pick up
Chemical Storage • Properly restrain ammonia gas cylinder within gas cabinet or fume hood at all times.
and Disposal • The ammonia cylinder must be stored upright, with tank valves are securely closed and valve protection cap in place, and firmly
secured to prevent falling or being knocked over.
• Protect the ammonia cylinder from physical damage; do not drag, roll, slide, or drop. Cylinder temperatures must not exceed 52
°C (125 °F).
Lab Specific Add lab-specific information not included above if needed (e.g., all work for this procedure is to take place in the designated fume
Information hood.)
• Engineering Controls/Equipment:
Conduct in a clean fume hood with a face velocity not less than 100 fpm.
The gas cylinder of ammonia, if small enough, must be placed in a fume hood and anchored using at least one chain before
dispensing the reagent. If the cylinder is too large for a normal hood, consider using a walk-in, with the cylinder anchored with
two chains.
All the reaction vessel joints (round bottom flask and cold finger) must be greased.
• PPE:
o Eye protection: PERSONS WITH POTENTIAL EXPOSURE TO AMMONIA MUST NOT WEAR CONTACT LENSES. Wear tight-fitting
safety goggles or safety glasses with side shields.
o Face Protection: Wear a face shield when the hood sash does not provide adequate protection.
o Hand protection: Wear a combination of flame resistant (FR) liner gloves, covered with a pair of chemical-resistant disposable
outer gloves (e.g. nitrile gloves or those specified in the specific SDS).The following products are approved FR Liners: Ansell
Kevlar® Goldknit® Lightweight 70-200 and Hanz Extremity Wear Nomex® Utility.
For gas release or for potential contact with larger quantities, use flame resistant (FR) liner gloves, covered with double nitrile or
heavier gauge nitrile or neoprene gloves.
Gloves must be inspected prior to use. Use proper glove removal technique (without touching glove's outer surface) to avoid
skin contact with this product. Remove gloves immediately upon contamination. Wash and dry hands after use.
o Clothing: Wear Nomex IIIA (NFPA 2112) lab coat; full length pants or equivalent; and close-toed and close-heeled shoes.
1. Properly restrain ammonia gas cylinder within fume hood at all times with at least one chain. Use also a ring clamp to secure the cylinder from the neck
just beneath the regulator.
2. Remove gas cap, confirm tank valve is closed, and remove bolt from regulator inlet.
3. Tightly insert appropriate regulator. Do not open gas tank valve.
4. Attach regulator to gas lines connected to the instrument/equipment. All lines must be chemically compatible with ammonia gas.
Step 2 – Dispensing and Condensing Anhydrous Ammonia into Reaction Flask (Figures 1 and 2)
NOTE: remember to grease all the reaction vessel joints (RBF and cold finger).
1. Flame dry glassware OR use glassware previously dried in an oven overnight at a minimum temperature of 120 ◦C.
2. Clamp a 2L round-bottom flask (RBF) with 2 necks. On one neck, fit cold finger. Put a septum on all the necks (cold finger and side arm).
3. Pierce the septum of the cold finger with a nitrogen inlet needle, and a vent needle on the side neck.
4. Purge the system with nitrogen for about 20 minutes.
5. Replace the nitrogen inlet needle on the cold finger with a needle that has been attached to a balloon apparatus, used to provide space for venting
ammonia gas.
6. Cool the flask down to < -40 °C (- 78 °C is an easier working temperature to keep the ammonia condensed). Ensure that a low temperature < -40 °C is
maintained throughout the procedure.
7. Fill the cold finger with dry ice and acetone.
8. Affix a long needle to the end of the tubing from the ammonia tank. Secure tubing by clamping it.
9. Pierce the needle into the septum of the RBF side neck and slowly open the valve on the ammonia tank. Set delivery pressure to 20 psig. This will begin the
transfer of ammonia to the reaction flask; ammonia will condense into the reaction flask (Figures 1 and 2).
10. Upon completion, close the regulator valve and the cylinder's valve, and remove the needle from the reaction flask. Vent the regulator before removing it.
Re-attach the cylinder's cap and allow the components to vent in the fume hood for at least 10 minutes
NOTE: If WR does not come in oil, it must be manipulated in a nitrogen-filled glovebox. Bring the WR (normally packaged under nitrogen) and
large pair of scissors or a knife, a suitably-sized container, and hexanes (distilled and degassed; anhydrous grade packaged under nitrogen can be
purchased from Acros or Sigma Aldrich) into the glovebox. Cut the block of WR into smaller pieces and submerge it in hexanes. Once in hexanes,
the WR can be removed from the glovebox and transferred (can be performed under air, away from water) to another container containing
mineral oil for long term storage.
1. Pieces (~2.5 g/piece) are transferred to a beaker containing hexanes that covers the metal fully.
2. Pieces are then washed with more hexanes to remove the oil and transferred to a second beaker containing more hexanes.
3. The pieces are flattened in the beaker containing hexanes then removed, washed with hexanes and transferred slowly to the reaction vessel containing
NH3(l).
4. The addition of the WR takes approximately 30 minutes. The rubber septum can be removed for short periods of time so the WR can be added into the
side neck. Addition of WR generates hydrogen gas which needs to escape the vessel. Insert a vent needle on the septum of the side neck. When the WR
contacts NH3(l), a brief hissing sound occurs as hydrogen gas is generated, and the solution turns dark blue. Pieces of WR must be added between 30−60
second intervals. As more WR is added, some splashing within the flask occurs, and the inside of the entire flask eventually becomes coated with a thin
layer of WR. After all WR has been added, replaced the nitrogen gas inlet with a balloon or a gas bubbler to monitor hydrogen gas evolution (Figure 3).
1. The alkyne is added as a neat solution directly into the reaction vessel using an automated syringe pump.
2. Set the addition rate to 1 mL/min, the addition must be directed into the center of the reaction mixture and not along the sides of the flask. The sides of
the flask have a layer of WR metal that can react with the alkyne in an exothermic manner, causing the septa to pop off.
1. Upon completion of the reaction, remove the cold finger and replace it with a large compatible tube directing the ammonia to the back of the fume hood.
2. Connect nitrogen to the side arm (Figure 4).
3. Keep the system under a continuous flow of nitrogen.
4. As ammonia evaporates, a layer of ice is formed on the flask which will keep the system cool as well as help to maintain a somewhat controlled rate of
evaporation (Figure 5).
5. When ~2/3 of the NH3(l) has evaporated, remove tubing and add slowly the desired amount of ether.
6. Cool the reaction vessel with an ice bath. Slowly add isopropanol to the reaction vessel to start quenching the WR, followed by the addition of methanol.
This will most likely get the reaction vessel to warm-up. If the solution begins to warm up, stop and allow it cool down before continuing the addition of the
quenching agent.
7. Be Very Careful with the addition of WATER! Even after methanol has been added, the water reactive agent can still react violently with water, especially if
there hasn't been sufficient mechanical stirring of the solution. Therefore, water must be add in small aliquots.
1. After the quenching process is completed, the mixture is diluted with ether, then filtered (gentle vacuum filtration) over celite (use a maximum of 500 mL
ether to rinse the flask and celite pad).
2. Transfer the biphasic filtrate to a 1 L separatory funnel and remove the aqueous layer. The organic layer is washed with brine (150−200 mL), dried over
anhydrous Na2SO4, and followed by gravity filtration.
3. The ether solvent is removed by distillation with mild heating (40−55˚C). The distillate normally contains a 1:1 mixture of product/ether. The use of a rotary
evaporator (rotovap) causes significant loss of product.