Dichloromethane → 1-(1-Benzothiophen-3-yl)ethan-1-ol
Reaction equation
[S:1]1[CH:5]=[C:4]([CH2:6][C:7](OC)=O)[C:3]2[CH:11]=[CH:12][CH:13]=[CH:14][C:2]1=2.[H-].[Al+3].[Li+].[H-].[H-].[H-].C(Cl)Cl.[O:24]1CCCC1>>[S:1]1[CH:5]=[C:4]([CH:6]([OH:24])[CH3:7])[C:3]2[CH:11]=[CH:12][CH:13]=[CH:14][C:2]1=2Participants
5
Procedure
A solution of methyl benzo[b]thiophen-3-ylacetate (69 g) in dry tetrahydrofuran (100 ml) was added dropwise to a suspension of lithium aluminium hydride (10 g) in dry tetrahydrofuran (500 ml) at room temperature followed by reflux for 1 h. Hydrolysis with water, filtration and removal of solvent gave an oil which was applied to a silica gel column (eluent: methylene chloride) giving 34.5 g of benzo[b]thiophen-3-ylethanol as an oil.
Workup
- temperatureby reflux for 1 h
- customHydrolysis
- filtrationwith water, filtration and removal of solvent
- customgave an oil which
Sources & evidence
- ORD record
- ord-d072f29a7e9c429f99669c130161e948
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06207677B1
Reaction notes
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