반응식
[N+:1](/[CH:4]=[CH:5]/[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)([O-:3])=[O:2].[BH4-].[Na+]>C(Cl)(Cl)Cl.C(O)(C)C>[N+:1]([CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)([O-:3])=[O:2]참가 물질
실험 절차
To a stirring mixture of trans-β-nitrostyrene (5.25 g, 0.035 mol) and silica gel (10 g, 230-400 mesh) in chloroform (400 mL) and isopropanol (75 mL) at room temperature, was slowly added sodium borohydride (5.50 g, 0.145 mol) over a period of 45 min. The reaction mixture was stirred for an additional 15 min and then carefully quenched with 10% hydrochloric acid (20 mL). Separated solid was filtered and washed with chloroform (50 mL). Combined filtrate and washing was washed with water (1×20 mL), brine (1×20 mL) and dried over anhydrous sodium sulfate. Solvent evaporation at reduced pressure gave a crude material which was purified by flash chromatography (silica gel, 8% ethyl acetate-hexane) to give 2.86 g of 1-nitro-2-phenylethane as a colorless oil (spicy odor); Rf (10% ethyl acetate in hexane) : 0.40; 1H-NMR (300 MHz, CDCl3) 7.40-7.20 (m, 5H), 4.60 (t, 2H), 3.30 (t, 2H).
후처리
- customof 45 min
- customcarefully quenched with 10% hydrochloric acid (20 mL)
- customSeparated solid
- filtrationwas filtered
- washwashed with chloroform (50 mL)
- washCombined filtrate and washing
- washwas washed with water (1×20 mL), brine (1×20 mL)
- dry with materialdried over anhydrous sodium sulfate
- customSolvent evaporation at reduced pressure
- customgave a crude material which
- customwas purified by flash chromatography (silica gel, 8% ethyl acetate-hexane)
출처 및 근거
- ORD 기록
- ord-28a296139c7544dcb942ea8c52facf62
- 출처 데이터셋
- uspto-grants-1998_11
- 특허 번호
- US05830870
연결된 노트
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