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

Nitric Acid → 5-Fluoro-7-nitroindole-2,3-dione

HRID 1470592
노트
인쇄 미리보기

반응식

HRID 1470592 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=[O:12].[N+:13]([O-])([OH:15])=[O:14]>OS(O)(=O)=O>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([N+:13]([O-:15])=[O:14])[CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 2365665-Fluoroisatin

생성물 1

HCID 167952125-Fluoro-7-nitroindole-2,3-dione수율 94.3%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a solution of 5-fluoro-1H-indole-2,3-dione (2.5 g, 15.0 mmol) in conc. H2SO4 (9 mL) was added very slowly fuming nitric acid (1.5 mL) at −5 to 0° C. The reaction mixture was stirred at the same temperature for one hour. After completion of the reaction, the reaction mixture was poured onto crushed ice and the resulting precipitate was filtered, washed with water (2-3 times) and dried under vacuum to obtain the title compound as yellow solid (3 g, 94.30%) which was used for the next step directly.

후처리

  1. customAfter completion of the reaction
  2. additionthe reaction mixture was poured
  3. customonto crushed ice
  4. filtrationthe resulting precipitate was filtered
  5. washwashed with water (2-3 times)
  6. customdried under vacuum

출처 및 근거

ORD 기록
ord-c62581fc360a4378a3109ff931816cfe
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006454B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트