Acetic Acid → HCID 69277781, compound
Reaction equation
C(O)(=[O:3])C.[F:5][C:6]([F:23])([F:22])[C:7]1[CH:21]=[CH:20][C:10]([CH2:11][S:12][C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=2)=[CH:9][CH:8]=1.OO.[OH2:26]>>[F:23][C:6]([F:5])([F:22])[C:7]1[CH:21]=[CH:20][C:10]([CH2:11][S:12]([C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=2)(=[O:3])=[O:26])=[CH:9][CH:8]=1Participants
5
Conditions
- Temperature
- 90 °C
Procedure
To a 15 ml of acetic acid solution of 2.23 g of 4-(4-trifluoromethylbenzylsulfanyl)phenol was added slowly, 2.5 ml of 30% hydrogen peroxide solution at approximately 80° C. The reaction mixture was stirred for 3 hours at 90° C., then poured into water, and the resulted precipitate was collected by filteration. After washing with water, the precipitate was dried by heating under the reduced pressure to produce 2.34 g of the desired product.
Workup
- customat approximately 80° C
- customthe resulted precipitate was collected by filteration
- washAfter washing with water
- customthe precipitate was dried
- temperatureby heating under the reduced pressure
Sources & evidence
- ORD record
- ord-48297c23f8614cf49ecc16a6c07d9cd8
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07470803B2
Reaction notes
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