Cyclohexanol → 2-Cyclohexyloxy-5-methanesulfonyl-benzoic acid
Reaction equation
Cl[C:2]1[CH:10]=[CH:9][C:8]([S:11]([CH3:14])(=[O:13])=[O:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH:15]1([OH:21])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1>>[CH:15]1([O:21][C:2]2[CH:10]=[CH:9][C:8]([S:11]([CH3:14])(=[O:13])=[O:12])=[CH:7][C:3]=2[C:4]([OH:6])=[O:5])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1Participants
3
Procedure
Prepared in analogy to Example A1 (b) from 2-chloro-5-methanesulfonyl-benzoic acid (Example A1(a)) and cyclohexanol. The crude material was purified by preparative HPLC to yield the title compound as a white solid. MS (m/e): 297.3 ([M−H]−, 100%).
Workup
- customThe crude material was purified by preparative HPLC
Sources & evidence
- ORD record
- ord-3ce9e7be7ff34546ab61c8b660f4b30c
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07220744B2
Reaction notes
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