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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → (E)-3-[4-(3-Pyridylmethyl)phenyl]acrylic acid methyl ester

HRID 2296045
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인쇄 미리보기

반응식

HRID 2296045 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]2[CH:15]=[CH:14][C:11]([CH:12]=O)=[CH:10][CH:9]=2)[CH:2]=1.[CH3:16][O:17][C:18]([CH:20]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:19]>C(Cl)(Cl)Cl>[CH3:16][O:17][C:18](=[O:19])/[CH:20]=[CH:12]/[C:11]1[CH:14]=[CH:15][C:8]([CH2:7][C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)=[CH:9][CH:10]=1
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참가 물질

4

반응물 2

HCID 17453Acetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 128821774-(3-Pyridylmethyl)benzaldehyde

생성물 1

HCID 12882181(E)-3-[4-(3-Pyridylmethyl)phenyl]acrylic acid methyl ester수율 45.3%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A mixture of 200 mg of 4-(3-pyridylmethyl)benzaldehyde (prepared as described in Reference Example 1), 0.14 g of methoxycarbonylmethylenetriphenylphosphorane and 5 ml of chloroform was stirred at room temperature for 3 days, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using methylene chloride as eluent to give 48 mg of the title compound having the following physical characteristics:

후처리

  1. concentrationconcentrated under reduced pressure
  2. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-12d0e5a5b1e342ec95620ceef573372a
출처 데이터셋
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04427682

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