Cyclohexanethiol → Methyl 3-bromo-6-(cyclohexylthiomethyl)-2-methoxybenzoate
Reaction equation
[Br:1][C:2]1[C:3]([OH:22])=[C:4]([C:9]([CH2:12][S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2OC)=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].Br[C:24]1C(OC)=C(C(CBr)=CC=1)C(OC)=O.C1(S)CCCCC1>>[Br:1][C:2]1[C:3]([O:22][CH3:24])=[C:4]([C:9]([CH2:12][S:13][CH:14]2[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]2)=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 82, starting from methyl 3-bromo-6-bromomethyl-2-methoxybenzoate (Intermediate 89) and cyclohexanethiol and used without further purification.
Workup
- customPrepared
- customused without further purification
Sources & evidence
- ORD record
- ord-51130e68260e45f3a5a3b1d0cfe11cd8
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067905B2
Reaction notes
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