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

Bromine → 6-Bromo-5-fluoroindoline

HRID 2214754
노트
인쇄 미리보기

반응식

HRID 2214754 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH2:6][CH2:5]2.[Br:11]Br>OS(O)(=O)=O.S([O-])([O-])(=O)=O.[Ag+2]>[Br:11][C:10]1[CH:9]=[C:8]2[C:4]([CH2:5][CH2:6][NH:7]2)=[CH:3][C:2]=1[F:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24408BromineHCID 27744635-Fluoroindoline

생성물 1

HCID 219483686-Bromo-5-fluoroindoline수율 89%

시약·촉매·용매 2

HCID 178418844HCID 178418844, 화합물촉매HCID 1118Sulfuric Acid용매

반응 조건

온도
-5 °C

실험 절차

A solution of 5-fluoroindoline (4.65 g, 34 mmole) in conc. H2SO4 acid (60 ml) under argon was treated with silver sulfate (5.5 g, 18 mmole) and stirred for 0.5 h, then cooled to −5° C. and treated dropwise over 15 min with bromine (5.6 g, 35 mmole). The mixture was maintained at −5° C. for 0.5 h, then allowed to warm to room temperature over 1 h, before adding cautiously to well stirred ice/water (600 ml). The mixture was filtered through Kieselguhr, then basified by addition of 40% NaOH solution and extracted with Et2O (2×300 ml). The combined extract was dried (Na2SO4) and concentrated under vacuum to afford the title compound as a beige solid (6.5 g, 89%). MH+ 216/218.

후처리

  1. temperatureThe mixture was maintained at −5° C. for 0.5 h
  2. temperatureto warm to room temperature over 1 h
  3. filtrationThe mixture was filtered through Kieselguhr
  4. additionbasified by addition of 40% NaOH solution
  5. extractionextracted with Et2O (2×300 ml)
  6. extractionThe combined extract
  7. dry with materialwas dried (Na2SO4)
  8. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-9184affec87f4713ad88711d89eb9a2d
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109201B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트