Sodium hydride → HCID 19390157, 화합물

HRID 1757264노트

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HRID 1757264 반응식
[Br-].[C:2]([CH2:4][CH2:5][CH2:6][CH2:7][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)#[N:3].[H-].[Na+].[S:29]1[CH:33]=[CH:32][C:31]([C:34]2[CH:35]=[C:36]([CH:39]=[CH:40][CH:41]=2)[CH:37]=O)=[CH:30]1>CN(C)C=O.O.C(O)(=O)C>[S:29]1[CH:33]=[CH:32][C:31]([C:34]2[CH:35]=[C:36](/[CH:37]=[CH:7]/[CH2:6][CH2:5][CH2:4][C:2]#[N:3])[CH:39]=[CH:40][CH:41]=2)=[CH:30]1

참가 물질

7

실험 절차

44.6 g of 4-cyanobutyltriphenylphosphonium bromide is dissolved in 250 ml of dimethylformamide, 4.2 g of 60% oily sodium hydride is added under ice cooling and stirring, then mixture is stirred at that temperature for 30 minutes, 18 g of 3-(3-thienyl)benzaldehyde is added, and the mixture is stirred at room temperature for further 20 hours. The reaction solution is diluted with water, acetic acid is added for neutralization, and then the solvent is distilled off under reduced pressure. The residue is led to two liquid phases using a system of water and ethyl ether, the organic layer is taken, washed with saturated saline and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. The residue is purified by silica gel column chromatography [Wako gel C-100, 500 g; hexane/ethyl acetate=4/1] to obtain 23.2 g (E)-6-[3-(3-thienyl)phenyl]-5-hexenenitrile as colorless oil.

후처리

  1. stirringmixture is stirred at that temperature for 30 minutes
  2. stirringthe mixture is stirred at room temperature for further 20 hours
  3. additionis added for neutralization
  4. distillationthe solvent is distilled off under reduced pressure
  5. washwashed with saturated saline
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationthe solvent is distilled off under reduced pressure
  8. customThe residue is purified by silica gel column chromatography [Wako gel C-100, 500 g; hexane/ethyl acetate=4/1]

출처 및 근거

ORD 기록
ord-be8a7ce2ba844e1e9ffcc3bd6bab0c25
출처 데이터셋
uspto-grants-1995_08
특허 번호
US05444084

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