반응식
[C:1]([C:3](=[CH:9][C:10]1[C:15]2[CH:16]=[CH:17][CH2:18][O:19][C:14]=2[C:13]([O:20][CH3:21])=[C:12]([O:22][CH3:23])[CH:11]=1)[C:4]([O:6][CH2:7][CH3:8])=[O:5])#[N:2].CC1C(Br)=C(O)C(Br)=CC=1C1(C2C=C(Br)C(O)=C(Br)C=2C)OS(=O)(=O)C2C=CC=CC1=2.C([BH3-])#N.[Na+].C(O)(=O)C>C(O)C>[C:1]([CH:3]([CH2:9][C:10]1[C:15]2[CH:16]=[CH:17][CH2:18][O:19][C:14]=2[C:13]([O:20][CH3:21])=[C:12]([O:22][CH3:23])[CH:11]=1)[C:4]([O:6][CH2:7][CH3:8])=[O:5])#[N:2]참가 물질
실험 절차
A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)-propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acidic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.
후처리
- temperatureHeating
- customthe ethanol removed under reduced pressure
- extractionsuccessively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL)
- dry with materialdried over magnesium sulfate
- customThe volatiles were removed under reduced pressure
- customto leave an amber oil, 18.22 g (91.4%) which
- customwas used without further purification
출처 및 근거
- ORD 기록
- ord-5465ba6dfefa4988b66fa1857a9e3d92
- 출처 데이터셋
- uspto-grants-1986_05
- 특허 번호
- US04587342
연결된 노트
불러오는 중…