Trichloroethanol → HCID 57215698, compound
Reaction equation
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[C:13]([C:14](Cl)=[O:15])=[CH:12][S:11][N:10]=2)[CH:4]=1.[Cl:19][C:20]([Cl:24])([Cl:23])[CH2:21][OH:22]>>[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[C:13]([C:14]([O:22][CH2:21][C:20]([Cl:24])([Cl:23])[Cl:19])=[O:15])=[CH:12][S:11][N:10]=2)[CH:4]=1Participants
3
Procedure
A solution of 2.0 g (0.0069 mol) of 3-(α,α,α-trifluoro-m-tolyl-4-isothiazolecarbonyl chloride and 1.22 g (1.18 equivalents) of 2,2,2-trichloroethanol was heated at 70°-140° in an oil bath for 6.5 hours. The reaction mixture was concentrated under vacuum to give 1.78 g of oil, nD23 =1.5499 (yield 63.8%).
Workup
- concentrationThe reaction mixture was concentrated under vacuum
Sources & evidence
- ORD record
- ord-446678bd3e61476187f5ce9da8a22cf5
- Source dataset
- uspto-grants-1980_02
- Patent number
- US04187099
Reaction notes
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