Sulfuric Acid → N-(3,5-dichloroalpha,alpha-dimethylbenzyl)formamide
Reaction equation
[C-]#[N:2].[Na+].S(=O)(=O)(O)O.[Cl:9][C:10]1[CH:11]=[C:12]([CH:17]=[C:18]([Cl:20])[CH:19]=1)[C:13](O)([CH3:15])[CH3:14].[C:21](=[O:24])([O-])[O-].[K+].[K+]>C(O)(=O)C>[Cl:9][C:10]1[CH:11]=[C:12]([CH:17]=[C:18]([Cl:20])[CH:19]=1)[C:13]([NH:2][CH:21]=[O:24])([CH3:15])[CH3:14]Participants
Procedure
To 7 ml of acetic acid, 2.83 g (57.8 mmol) of sodium cyanide was gradually added at a temperature not higher than 20° C. To the suspension thereby obtained, 7 ml of an acetic acid solution of 7 ml of concentrated sulfuric acid was dropwise added at not higher than 20° C., and the mixture was stirred at room temperature for one hour. Then, 10.3 g (50 mmol) of 3,5-dichloro-α,α-dimethylbenzyl alcohol was dropwise added thereto at not higher than 20° C. The reaction mixture was stirred at room temperature for two days, and then poured into ice water. The mixture was alkalified with potassium carbonate and extracted with ethyl acetate. The ethyl acetate solution was washed with water, dried and then concentrated. The solid thereby obtained was washed with n-hexane and collected by filtration to obtain 8.2 g (yield: 70.7%) of N-(3,5-dichloro-α,α-dimethylbenzyl)formamide as white needle-like crystals.
Workup
- customTo the suspension thereby obtained
- customhigher than 20° C
- stirringThe reaction mixture was stirred at room temperature for two days
- extractionextracted with ethyl acetate
- washThe ethyl acetate solution was washed with water
- customdried
- concentrationconcentrated
- customThe solid thereby obtained
- washwas washed with n-hexane
- filtrationcollected by filtration
Sources & evidence
- ORD record
- ord-fb9b13519209462390d6df56119e250b
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05076834
Reaction notes
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