Ethanol, reaction products with ammonia, distn. residues → HCID 21996512, 화합물

HRID 1977984노트

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HRID 1977984 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][CH2:9][C:10]2=[CH:13][C:14]#[N:15])=[CH:5][CH:4]=1.N.C(O)C>C(O)C.[Co]>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][CH2:9]/[C:10]/2=[CH:13]/[C:14]#[N:15])=[CH:5][CH:4]=1

참가 물질

5

실험 절차

To a solution of (1,2,3,4-tetrahydro-7-methoxy-1-naphthylidene)acetonitrile (4.0 g, 20 mmol) in ethanol (10 ml) were added a saturated ammonia/ethanol solution (5 ml) and Raney cobalt (ODHT-60, 1 g). The reaction mixture was stirred for 3.5 hours at room temperature under hydrogen atmosphere (about 4 kgf/cm2). The Raney cobalt was filtered off, then the solvent was distilled off under reduced pressure. To the residue was added dilute hydrochloric acid, then the organic layer was subjected to extraction with ethyl acetate. The extract solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and water, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography to give the above-titled compound (yield 2.14 g, oil).

후처리

  1. filtrationThe Raney cobalt was filtered off
  2. distillationthe solvent was distilled off under reduced pressure
  3. additionTo the residue was added dilute hydrochloric acid
  4. extractionthe organic layer was subjected to extraction with ethyl acetate
  5. washThe extract solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and water, which
  6. dry with materialwas dried over anhydrous magnesium sulfate
  7. distillationby distilling off the solvent under reduced pressure
  8. customThe residue was purified by means of a silica gel column chromatography

출처 및 근거

ORD 기록
ord-31d3ae4f705a461cacd3bfd4b17bbbba
출처 데이터셋
uspto-grants-2001_05
특허 번호
US06235789B1

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