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

Methanol → 2-Amino-6-nitro-benzoic acid

HRID 76848
노트
인쇄 미리보기

반응식

HRID 76848 반응식
[N+:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-])=O)[C:5]=1[C:6]([OH:8])=[O:7])([O-:3])=[O:2].[SH-].[Na+].CO>O>[NH2:13][C:9]1[CH:10]=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]=1[C:6]([OH:8])=[O:7]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 28015Sodium hydrosulfideHCID 119206Benzoic acid, 2,6-dinitro-

생성물 1

HCID 957952-Amino-6-nitro-benzoic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

In one non-limiting reaction scheme, dinitrobenzoic acid may be reacted with about one to about five equivalents of an alkali hydrosulfide in a methanol:water mixture at reflux temperature for about 20 to about 40 minutes to produce an aminonitrobenzoic acid. As is described in the Example below, 2,6-dinitrobenzoic acid may be allowed to react with about three equivalents of sodium hydrosulfide in a methanol:water mixture at reflux temperature for about 30 minutes to produce 2-amino-6-nitrobenzoic acid. In some non-limiting embodiments, three equivalents of sodium hydrosulfide may be reacted with one equivalent of the sodium salt of 2,6-dinitrobenzoic acid in refluxing methanol/water followed by acidification.

출처 및 근거

ORD 기록
ord-69bad618805b4b82beaba1d05b555cee
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835677B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트