4-Bromophenol → (2S)-2-(4-bromophenoxy)propanoic acid, ethyl ester
Reaction equation
CCOC(/N=N/C(OCC)=O)=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:32]([O:37][CH2:38][CH3:39])(=[O:36])[C@@H:33]([CH3:35])[OH:34].[Br:40][C:41]1[CH:46]=[CH:45][C:44](O)=[CH:43][CH:42]=1>O1CCCC1>[Br:40][C:41]1[CH:46]=[CH:45][C:44]([O:34][C@@H:33]([CH3:35])[C:32]([O:37][CH2:38][CH3:39])=[O:36])=[CH:43][CH:42]=1Participants
6
Procedure
Prepared according to the method described in Example 1a) from diethylazodicarboxylate (6.7 ml), triphenylphosphine (13.11 g), (R)-(+)-ethyl lactate (5.67 ml) and 4-bromophenol (8.65 g) in dry tetrahydrofuran (125 ml). The residue obtained after work-up was purified by column chromatography over silica eluting with isohexane:dichloromethane (2:3) to give the sub-title compound as an oil (12.2 g).
Workup
- customPrepared
- customThe residue obtained after work-up
- customwas purified by column chromatography over silica eluting with isohexane:dichloromethane (2:3)
Sources & evidence
- ORD record
- ord-e639739a1c3d4e48abee8a3c6cdade37
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300352B1
Reaction notes
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