2-(3-Bromophenyl)ethan-1-ol → Benzeneethanol, 3-bromo-, 1-methanesulfonate
Reaction equation
[CH3:1][S:2]([O:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([N+]([O-])=O)[CH:9]=1)(=[O:4])=[O:3].[Br:17]C1C=C(CCO)C=CC=1>>[CH3:1][S:2]([O:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([Br:17])[CH:9]=1)(=[O:4])=[O:3]Participants
3
Procedure
The title compound was prepared in 77% yield using a similar procedure to description D4 starting from 2-(3-bromophenyl)ethanol.
Sources & evidence
- ORD record
- ord-87c9a193199e465b98dde7bdfc7df08f
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07279481B2
Reaction notes
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