Sodium borohydride → Methyl 3-(1-Hydroxyethyl)benzoate
반응식
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10](=[O:12])[CH3:11])[CH:5]=1.[BH4-].[Na+]>CCO>[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([OH:12])[CH3:11])[CH:5]=1참가 물질
실험 절차
General Procedure EE: Into the EtOH (70 ml) solution of methyl-3-acetylbenzoate (771 mg, 3.98 mmol) was added sodium borohydride (232 mg, 6.09 mmol). The mixture was stirred at rt under an atmosphere of nitrogen for one hour. After that time, the mixture was quenched with saturated NH4Cl followed by water, extracted with EtOAc (3×50 ml). The extracts were washed with water (50 ml), brine (50 ml), dried over MgSO4. After concentrated in vacuo, a beige oil (6269-42, 700 mg) was obtained. It was purified by chromatography on silica gel (25 g) eluting with 20% (200 ml), 30% (200 ml) and 40% EtOAc/hexane (200 ml) to give the title compound as a colorless oil (504 mg, 67% yield). TLC: Rf=0.41 (eluting with 30% EtOAc/hexane). 1H NMR (400 MHz, CDCl3): δ=1.52 (d, J=6.4 Hz, 3H), 1.89 (d, J=4.0 Hz, 1H), 3.92 (s, 3H), 4.93-5.01 (m, 1H), 7.43 (t, J=8.0 Hz, 1H), 7.59 (md, J=8.0 Hz, 1H), 7.95 (td, J=1.6 & 8.0 Hz, 1H), 8.03-8.05 (m, 1H). MS (ES+): m/z 181.19 [MH+]. HPLC: tR=2.51 min (polar—5 min, ZQ3).
후처리
- customAfter that time, the mixture was quenched with saturated NH4Cl
- extractionextracted with EtOAc (3×50 ml)
- washThe extracts were washed with water (50 ml), brine (50 ml)
- dry with materialdried over MgSO4
- concentrationAfter concentrated in vacuo
- customa beige oil (6269-42, 700 mg) was obtained
- customIt was purified by chromatography on silica gel (25 g)
- washeluting with 20% (200 ml), 30% (200 ml) and 40% EtOAc/hexane (200 ml)
출처 및 근거
- ORD 기록
- ord-2ad6df53f6964e7cb49e3064ae458806
- 출처 데이터셋
- uspto-grants-2011_09
- 특허 번호
- US08022206B2
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