Hydrochloric Acid → 4,4,4-Trifluorobutyl thioacetate
Reaction equation
I[CH2:2][CH2:3][CH2:4][C:5]([F:8])([F:7])[F:6].[C:9]([O-:12])(=[S:11])[CH3:10].[K+].Cl>CN(C)C=O>[C:9]([O:12][CH2:2][CH2:3][CH2:4][C:5]([F:8])([F:7])[F:6])(=[S:11])[CH3:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A mixture of 23.80 g of 1-iodo-4,4,4-trifluorobutane, 100 ml of N,N-dimethylformamide and 11.42 g of potassium thioacetate was heated and stirred at 80° C. for 4 hours under a nitrogen atmosphere. A reaction vessel was cooled in an ice bath. To the reaction mixture was added an aqueous 1N hydrochloric acid solution, and the mixture was extracted with 100 ml of t-butyl methyl ether twice. Organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over sodium sulfate, filtered, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 18.20 g of 4,4,4-trifluorobutyl thioacetate represented by the formula:
Workup
- temperaturewas heated
- temperatureA reaction vessel was cooled in an ice bath
- extractionthe mixture was extracted with 100 ml of t-butyl methyl ether twice
- washwashed with an aqueous saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-0e41ff9cecd64e4b89e4f03e0560501c
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247596B2
Reaction notes
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