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

Acetamide → Methyl 6-benzoyloxyhexanoate

HRID 21918
노트
인쇄 미리보기

반응식

HRID 21918 반응식
[C:1]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH:14](Br)[C:15]([O:17][CH3:18])=[O:16])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F-:20].[K+].C(N)(=O)C>>[C:1]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH:14]([F:20])[C:15]([O:17][CH3:18])=[O:16])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:1]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([O:17][CH3:18])=[O:16])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 178AcetamideHCID 522689Potassium FluorideHCID 15222235methyl 6-benzoyloxy-2(RS)-bromohexanoate

생성물 2

HCID 15224608methyl 6-benzoyloxy-2(RS)-fluorohexanoateHCID 19930972Methyl 6-benzoyloxyhexanoate수율 58.3%

반응 조건

온도
105 °C

실험 절차

A mixture of methyl 6-benzoyloxy-2(RS)-bromo-hexanoate (e) (14.02 g), potassium fluoride (12.59 g) and acetamide (12.3 g) was stirred at 105° C. for 6 hours. The crude product obtained by treating in the conventional manner was subjected to silica gel chromatography to give the title compound (f) and methyl 6-benzoyloxyhexanoate (g) (3.11 g, yield: 29%).

후처리

  1. customThe crude product obtained
  2. additionby treating in the conventional manner

출처 및 근거

ORD 기록
ord-beec5d027b5441a18961f0be48c28101
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05426115

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트