Tetrahydrofuran → HCID 18953814, 화합물

HRID 1491828노트

반응식

HRID 1491828 반응식
[C:1]([C:4]1[N:9]=[C:8]([CH:10]=[O:11])[CH:7]=[CH:6][CH:5]=1)(=O)[CH3:2].[C:12](C=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)#[N:13].O1CCC[CH2:35]1>>[C:10]([C:8]1[CH:7]=[CH:6][CH:5]=[C:4](/[CH:1]=[CH:2]/[C:12]#[N:13])[N:9]=1)(=[O:11])[CH3:35]

참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 85524(Triphenylphosphoranylidene)acetonitrileHCID 189538106-Acetylpyridine-2-carbaldehyde

생성물 1

HCID 18953814HCID 18953814, 화합물

실험 절차

A mixture of 6-acetyl-2-pyridinecarbaldehyde (0.5 g) and cyanomethylenetriphenylphosphorane (1.5 g) in tetrahydrofuran (5 ml) was stirred for 6 hours and the mixture was evaporated in vacuo. The residue was separated and purified by column chromatography on silica gel and eluted with a mixture of n-hexane and ethyl acetate (4:1, V/V). The eluted fast fractions containing the desired product were collected and evaporated in vacuo to give 2-acetyl-6-[2-(E)-cyanovinyl]pyridine (0.18 g).

후처리

  1. customthe mixture was evaporated in vacuo
  2. customThe residue was separated
  3. custompurified by column chromatography on silica gel
  4. washeluted with a mixture of n-hexane and ethyl acetate (4:1, V/V)
  5. washThe eluted fast fractions
  6. additioncontaining the desired product
  7. customwere collected
  8. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-6efd63d9edd34c91a3ad9d609ad7069a
출처 데이터셋
uspto-grants-1994_12
특허 번호
US05371097

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