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

2-Acetamido-5-methoxy-4-nitrobenzoic acid → 2-Amino-4-nitro-5-methoxybenzoic Acid

HRID 634740
노트
인쇄 미리보기

반응식

HRID 634740 반응식
C([NH:4][C:5]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[C:11]([O:17][CH3:18])=[CH:10][C:6]=1[C:7]([OH:9])=[O:8])(=O)C>O.Cl>[NH2:4][C:5]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[C:11]([O:17][CH3:18])=[CH:10][C:6]=1[C:7]([OH:9])=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 212603512-Acetamido-5-methoxy-4-nitrobenzoic acid

생성물 1

HCID 212602732-Amino-4-nitro-5-methoxybenzoic Acid수율 92%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

반응 조건

온도
0 °C

실험 절차

A solution of 2-acetamido-5-methoxy-4-nitrobenzoic acid (21.6 g, 85 mmol) in water (76 ml) and concentrated hydrochloric acid (30.5 ml) was heated at reflux for 3 hours. The reaction mixture was cooled to 0° C., the resulting solid was collected by filtration, washed with water and dried under vacuum to give 2-amino-5-methoxy-4-nitrobenzoic acid (I 6.6 g, 92%).

후처리

  1. temperatureat reflux for 3 hours
  2. filtrationthe resulting solid was collected by filtration
  3. washwashed with water
  4. customdried under vacuum

출처 및 근거

ORD 기록
ord-81d073c9ba1f4d358902b3c0b4520d2f
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06184225B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트