Hydrochloric Acid → (2E)-3-(2-Chlorophenyl)-2-propen-1-ol
Reaction equation
[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[CH:4]=[CH:5][C:6](O)=[O:7].[BH4-].[Na+].Cl>C1COCC1>[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1/[CH:4]=[CH:5]/[CH2:6][OH:7]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-chlorocinnamic acid (5.00 g, 27.4 mmol) in THF (50 mL) was slowly added to a suspension of NaBH4 (1.24 g, 32.9 mmol) in THF (50 mL) at room temperature. The mixture was stirred until evolution of gas ceased. A solution of 12 (3.47 g, 13.7 mmol) in THF (50 mL) was then added and the mixture was stirred at room temperature for 1 h. Aqueous 3 N HCl solution (10 mL) was added carefully and the mixture was extracted with Et2O. The combined organic layers were successively washed with aqueous 1 N NaOH solution and brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (CH2Cl2:(CH3)2CO, 95:5) to yield the title compound (2.86 g, 62% yield).
Workup
- stirringthe mixture was stirred at room temperature for 1 h
- extractionthe mixture was extracted with Et2O
- washThe combined organic layers were successively washed with aqueous 1 N NaOH solution and brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by flash chromatography (CH2Cl2:(CH3)2CO, 95:5)
Sources & evidence
- ORD record
- ord-daccbe0c24cc482e9c196d91f09bd1c1
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07642277B2
Reaction notes
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