Thionyl Chloride → 2-(4-(Trifluoromethyl)phenyl)acetyl chloride
Reaction equation
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10](O)=[O:11])=[CH:5][CH:4]=1.S(Cl)([Cl:17])=O>>[F:1][C:2]([F:14])([F:13])[C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([Cl:17])=[O:11])=[CH:5][CH:4]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
Under an argon atmosphere, to 4-trifluoromethylphenylacetic acid (51) (817 mg, 4.00 mmol) was added thionyl chloride (5.00 mL, 68.9 mmol), and heated to reflux (100° C.) for 1.5 h. After cooling to room temperature, the mixture was concentrated under reduced pressure to give 4-trifluoromethylphenylacetyl chloride (52) as a brown oily crude product, which was used in the next reaction without further purification.
Workup
- temperatureheated
- temperatureAfter cooling to room temperature
- concentrationthe mixture was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-c744af468a934165965890c8dd28c1f2
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546568B2
Reaction notes
Loading…