Water → HCID 54018396, compound
Reaction equation
[CH3:1][C:2]([CH3:18])([CH:4]1[CH:8]([CH3:9])[O:7][C:6]([C:14]([Cl:17])([F:16])[F:15])([C:10]([Cl:13])([F:12])[F:11])[O:5]1)[OH:3].[O-:19][C:20]#[N:21].[Na+].FC(F)(F)C(O)=O.O>C(Cl)Cl>[C:20]([O:3][C:2]([CH3:1])([CH3:18])[CH:4]1[CH:8]([CH3:9])[O:7][C:6]([C:14]([Cl:17])([F:16])[F:15])([C:10]([Cl:13])([F:11])[F:12])[O:5]1)(=[O:19])[NH2:21]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 31.5 grams (0.1 mol) of α,α,5-trimethyl-2,2-bis(chlorodifluoromethyl)-1,3-dioxolane-4-methanol in 180 ml methylene dichloride is treated with 13.0 grams sodium cyanate (0.2 mol) while 22.8 grams of trifluoroacetic acid (0.2 mol) is added dropwise. The reaction is carried out at 25°-35° C. for 24 hours. After the reaction is completed, a small amount of water is added to dissolve salts and the methylene dichloride solution is separated and extracted once more with water. Vacuum stripping yields the product α,α,5-trimethyl-2,2-bis(chlorodifluoromethyl)-1,3-dioxolane-4-methanol carbamate. The product is purified by crystallization from a mixture of benzene and hexane.
Workup
- additionis added dropwise
- dissolutionto dissolve salts
- customthe methylene dichloride solution is separated
- extractionextracted once more with water
Sources & evidence
- ORD record
- ord-118ffb46428c478ca3a0574c2c436917
- Source dataset
- uspto-grants-1976_12
- Patent number
- US03996376
Reaction notes
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