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

3,4-Dimethoxy-2-nitrobenzoic acid → 2-Amino-3,4-dimethoxybenzoic acid

HRID 354831
노트
인쇄 미리보기

반응식

HRID 354831 반응식
[CH3:1][O:2][C:3]1[C:4]([N+:14]([O-])=O)=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:6]([OH:8])=[O:7].[H][H]>[OH-].[NH4+].[Pd]>[CH3:1][O:2][C:3]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:5]([C:6]([OH:8])=[O:7])[C:4]=1[NH2:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 12522693,4-Dimethoxy-2-nitrobenzoic acidHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 117455912-Amino-3,4-dimethoxybenzoic acid수율 78.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 14923Ammonium Hydroxide용매

실험 절차

A solution of 3,4-dimethoxy-2-nitro benzoic acid (1011 g., 4.45 moles) in 14 liters of 1.3 N ammonium hydroxide was reduced at 60 psi in presence of 60 grams of palladium on barium carbonate. Hydrogen uptake ceased after four hours. The reaction mixture was filtered through diatomaceous earth and acidified with glacial acetic acid (1.2 liters) to yield 685 grams (78%) of the anthranilic acid, M.P. 183°-184° C.

후처리

  1. filtrationThe reaction mixture was filtered through diatomaceous earth

출처 및 근거

ORD 기록
ord-9f9306c19b6b4f69a7f9343fbd0387ff
출처 데이터셋
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04377581

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트