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

HCID 178488256, 화합물 → HCID 178526501, 화합물

HRID 274517
노트
인쇄 미리보기

반응식

HRID 274517 반응식
C[O:2][C:3]1[CH:8]=[C:7]([C:9]2[NH:13][N:12]=[N:11][N:10]=2)[CH:6]=[C:5]([N+:14]([O-:16])=[O:15])[C:4]=1[OH:17]>Br>[N+:14]([C:5]1[CH:6]=[C:7]([C:9]2[NH:13][N:12]=[N:11][N:10]=2)[CH:8]=[C:3]([OH:2])[C:4]=1[OH:17])([O-:16])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178488256HCID 178488256, 화합물

생성물 1

HCID 178526501HCID 178526501, 화합물

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

실험 절차

4.0 g of 2-methoxy-6-nitro-4-(1H-tetrazol-5-yl)phenol are treated with 40 ml of constant-boiling hydrobromic acid, whereupon the mixture is stirred at 140° for 8 hours under a nitrogen atmostphere. After cooling, the mixture is poured on to ice. The separated precipitate is filtered under suction and recrystallized from ether. There is obtained 3-nitro-5-(1H-tetrazol-5-yl)-pyrocatechol in the form of orange crystals of m.p. >240° (dec.).

후처리

  1. temperatureAfter cooling
  2. additionthe mixture is poured on to ice
  3. filtrationThe separated precipitate is filtered under suction
  4. customrecrystallized from ether

출처 및 근거

ORD 기록
ord-823254dc0881453192b91afeee2c884e
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05389653

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트