tert-Butyl mercaptan → [3-(4-Bromo-2-tert-butylsulfanylmethyl-phenoxy)-4-methoxy-phenyl]-acetic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4](=[O:24])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18]([Br:21])=[CH:17][C:16]=2[CH2:22]Br)[CH:7]=1)[CH3:2].[CH3:25][C:26]([SH:29])([CH3:28])[CH3:27]>>[CH2:1]([O:3][C:4](=[O:24])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18]([Br:21])=[CH:17][C:16]=2[CH2:22][S:29][C:26]([CH3:28])([CH3:27])[CH3:25])[CH:7]=1)[CH3:2]Participants
3
Procedure
Prepared according to the procedure described in Example 15, Step 5, using the following starting materials: [3-(4-bromo-2-bromomethyl-phenoxy)-4-methoxy-phenyl]-acetic acid ethyl ester and 2-methyl-2-propanethiol.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-e81cf8be77254cf08c024393555f5ccb
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08071807B2
Reaction notes
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