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

N1-(5-chloro-2-methoxy-4-nitrophenyl)acetamide → 5-Chloro-2-methoxy-4-nitroaniline

HRID 2057573
노트
인쇄 미리보기

반응식

HRID 2057573 반응식
C([NH:4][C:5]1[CH:10]=[C:9]([Cl:11])[C:8]([N+:12]([O-:14])=[O:13])=[CH:7][C:6]=1[O:15][CH3:16])(=O)C>[OH-].[K+]>[NH2:4][C:5]1[CH:10]=[C:9]([Cl:11])[C:8]([N+:12]([O-:14])=[O:13])=[CH:7][C:6]=1[O:15][CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 2775778N1-(5-chloro-2-methoxy-4-nitrophenyl)acetamide

생성물 1

HCID 804105-Chloro-2-methoxy-4-nitroaniline

시약·촉매·용매 1

HCID 14797Potassium Hydroxide용매

실험 절차

0.5 mol (99.5 g) of 2-acetamido-4-chloro-5-nitroanisole and 125 ml of a solution of potassium hydroxide (140 g of KOH/100 ml of water) are introduced into a 500 ml flask; the mixture is brought to between 100° and 110° C. for one hour and three quarters; the product is dried without heating and washed with water.

후처리

  1. customthe product is dried
  2. temperaturewithout heating
  3. washwashed with water

출처 및 근거

ORD 기록
ord-c6dbbc4a161a46cb97be7a9cb9ce295a
출처 데이터셋
uspto-grants-1980_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04211776

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트