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

Acetaminophen → 4'-Allyloxyacetanilide

HRID 361698
노트
인쇄 미리보기

반응식

HRID 361698 반응식
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[CH2:12](Br)[CH:13]=[CH2:14].C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:14][CH:13]=[CH2:12])=[CH:7][CH:6]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1983AcetaminophenHCID 7841Allyl bromideHCID 11430Potassium Carbonate

생성물 1

HCID 231034'-Allyloxyacetanilide

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

Commercially available 4-acetamido phenol (1 molar equivalent), allyl bromide (1 molar equivalent) and potassium carbonate (1 molar equivalent) in butan-2-one were heated at reflux for 18 hours with stirring. The mixture was cooled, filtered and the solid residue washed with ether. The combined filtrates were evaporated and the solid residue was further purified by crystallisation from ethyl acetate-hexane to give 4-acetamido-1-allyloxy benzene as a colourless solid, m.p. 85°-86° C.

후처리

  1. temperatureat reflux for 18 hours
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. washthe solid residue washed with ether
  5. customThe combined filtrates were evaporated
  6. customthe solid residue was further purified by crystallisation from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-00d330a9d291460891b62d2b6f79ce4c
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05866611

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트