Methyl Salicylate → HCID 10491482, compound
Reaction equation
[C:1]([O:10][CH3:11])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[Br:12][CH2:13][CH2:14]Br>>[Br:12][CH2:13][CH2:14][O:4][C:3]1[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[C:1]([O:10][CH3:11])=[O:9]Participants
3
Procedure
The subtitle compound was prepared from methyl salicylate (5 g) and 1,2-dibromoethane (30.67 g) by the method of example 21 step (ii). Purified by chromatography eluting with 10% ethyl acetate in isohexane. Yield 4.9 g.
Workup
- customPurified by chromatography
- washeluting with 10% ethyl acetate in isohexane
Sources & evidence
- ORD record
- ord-5fed13dcd268491ba2c2162277821d84
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06200981B1
Reaction notes
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