Sodium borohydride → Methyl 3-(1-Hydroxyethyl)benzoate
反応式
[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]=1参加物
実験手順
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).
後処理
- 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)
出典と根拠
- ORDレコード
- ord-2ad6df53f6964e7cb49e3064ae458806
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08022206B2
反応ノート
読み込み中…