Water → 3-Acetoxy-4-trifluoromethyl-benzoic acid
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11]([F:14])([F:13])[F:12])[C:5]([OH:7])=[O:6].O.[C:16](OC(=O)C)(=[O:18])[CH3:17]>>[C:16]([O:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11]([F:12])([F:13])[F:14])[C:5]([OH:7])=[O:6])(=[O:18])[CH3:17]Participants
4
Procedure
3.5 g (17 mmol) of 3-hydroxy-4-trifluoromethyl-benzoic acid (prepared as described in WO 2006/128184) were dissolved in 35 ml of acetic acid anhydride and heated to reflux for 3 h. 60 ml of water were added and heating to reflux was continued for 10 min. After cooling and stirring overnight, the formed precipitate was collected by suction and dried to give 3.0 g of the title compound.
Workup
- temperatureheated
- temperatureto reflux for 3 h
- temperatureheating
- temperatureto reflux
- temperatureAfter cooling
- customthe formed precipitate was collected by suction
- customdried
Sources & evidence
- ORD record
- ord-957a9001908f4cabab4b9c44098245c7
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08445530B2
Reaction notes
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