홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → 3-(6-Bromopyridin-3-yl)acrylic acid methyl ester

HRID 238306
노트
인쇄 미리보기

반응식

HRID 238306 반응식
[CH3:1][O:2][C:3](=[O:24])[CH:4]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Br:25][C:26]1[N:31]=[CH:30][C:29]([CH:32]=O)=[CH:28][CH:27]=1>C1COCC1>[CH3:1][O:2][C:3](=[O:24])[CH:4]=[CH:32][C:29]1[CH:30]=[N:31][C:26]([Br:25])=[CH:27][CH:28]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 17453Acetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 117692346-Bromo-3-pyridinecarboxaldehyde

생성물 1

HCID 714275823-(6-Bromopyridin-3-yl)acrylic acid methyl ester수율 90.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

20 g (59.8 mmol) of 2-(triphenylphosphoranylidene)acetic acid methyl ester were added, by portion, to a solution of 11.1 g (59.8 mmol) of 6-bromopyridine-3-carbaldehyde in anhydrous THF at 0° C. The mixture was stirred at 0° C. to room temperature for 4 h. The solvent was removed in vacuo and the residue was purified by chromatography (silica gel, cyclohexane/ethyl acetate 95:5) to give 13.1 g (90.4%) of the title compound (trans/cis ratio 95:5) as a white solid.

후처리

  1. customThe solvent was removed in vacuo
  2. customthe residue was purified by chromatography (silica gel, cyclohexane/ethyl acetate 95:5)

출처 및 근거

ORD 기록
ord-6e25989d1f154dda99f1e1a3990c1631
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642620B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트