Chlorosulfonic acid → 1403387-05-2
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([O:11][CH3:12])=[O:10])[CH:5]=[CH:6][CH:7]=1.[Cl:13][S:14](O)(=[O:16])=[O:15]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:14]([Cl:13])(=[O:16])=[O:15])=[C:4]([CH2:8][C:9]([O:11][CH3:12])=[O:10])[CH:3]=1Participants
3
Procedure
Methyl 2-(3-bromophenyl)acetate (22 g, 67 mmol) was slowly added into ClSO3H at −10° C. After 1 h, the mixture was warmed up to rt and stirred overnight, diluted slowly with ice water and extracted with EA. The organic layer was washed with water, dried over Na2SO4 and evaporated to give compound P15a (17 g, 54%).
Workup
- extractionextracted with EA
- washThe organic layer was washed with water
- dry with materialdried over Na2SO4
- customevaporated
- customto give compound P15a (17 g, 54%)
Sources & evidence
- ORD record
- ord-6bdd0a8009b1423cbe5b959f58aecfca
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946446B2
Reaction notes
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