반응식
[CH:1]1[C:2]2[CH:22]=[CH:21][C:20]3[C:19]4[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=4[CH:13]=[CH:12][C:11]=3[C:3]=2[O:4][C:5]=1[C:6](OCC)=[O:7].[BH4-].[Li+].C1COCC1.Cl>O>[CH:1]1[C:2]2[CH:22]=[CH:21][C:20]3[C:19]4[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=4[CH:13]=[CH:12][C:11]=3[C:3]=2[O:4][C:5]=1[CH2:6][OH:7]참가 물질
실험 절차
To a RB flask equipped with magnetic stirring bar, reflux condenser and N2 inlet tube with bubbler was added ethyl phenanthro[1,2-b]furan-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc., 7.9 g, 27.2 mmol), lithium borohydride (Aldrich, 0.65 g, 30 mmol) and dry THF (400 mL). The mixture was stirred at reflux for 6 h and then poured into H2O (1 L). The reaction mixture was acidified with 1N HCl and the resulting white solid was filtered, washed with additional H2O (1500 mL) then dissolved in CH2Cl2 (500 mL), dried (Na2SO4), filtered, concentrated to 200 mL and diluted to 500 mL with hexane. The resulting material was filtered, washed with hexane (100 mL) and placed in a vacuum oven overnight. A total of 6.1 g (90.1%) of phenanthro[1,2-b]-furan-2-methanol, mp 125°-126° , was obtained (C,H).
후처리
- customTo a RB flask equipped with magnetic stirring bar
- temperaturereflux condenser and N2 inlet tube with bubbler
- temperatureat reflux for 6 h
- filtrationthe resulting white solid was filtered
- washwashed with additional H2O (1500 mL)
- dissolutionthen dissolved in CH2Cl2 (500 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated to 200 mL
- additiondiluted to 500 mL with hexane
- filtrationThe resulting material was filtered
- washwashed with hexane (100 mL)
- customplaced in a vacuum oven overnight
출처 및 근거
- ORD 기록
- ord-61e93e598362434f9130f8b2ebef0276
- 출처 데이터셋
- uspto-grants-1991_03
- 특허 번호
- US04999369
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