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

Phosphorus oxychloride → Isoquinoline, 1-chloro-

HRID 1820566
노트
인쇄 미리보기

반응식

HRID 1820566 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N+:2]=1[O-].P(Cl)(Cl)([Cl:14])=O>C(Cl)(Cl)Cl>[Cl:14][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 290378isoquinolin-N-oxide

생성물 1

HCID 140539Isoquinoline, 1-chloro-수율 48.4%

시약·촉매·용매 1

HCID 6212Chloroform용매

반응 조건

온도
17.5 °C

실험 절차

69.3 g of isoquinoline N-oxide (448 mmol) manufactured by Tokyo Chemical Industry Co., Ltd. and 225 ml of chloroform were introduced into a 1 L-three-neck flask dissolved therein. Then, 219.6 g (1,432 mmol) of phosphorous oxychloride was slowly added dropwise therein and stirred under ice-cooling while maintaining the inner temperature at 15 to 20° C. Thereafter, the mixture was heated and stirred under reflux for 3 hours. The reaction product was left to cool to room temperature, and the resulting product was poured into ice water. The mixture was extracted with ethyl acetate, and the organic layer was washed with water until it was neutral. The solvent was then dried under reduced pressure. The residue was purified using silica gel column chromatography (eluent: chloroform/hexane: 5/1) to yield 35.5 g of 1-chloroisoquinoline white crystals (44.9% yield).

후처리

  1. dissolutiondissolved
  2. temperaturecooling
  3. temperatureThereafter, the mixture was heated
  4. stirringstirred
  5. temperatureunder reflux for 3 hours
  6. waitThe reaction product was left
  7. temperatureto cool to room temperature
  8. extractionThe mixture was extracted with ethyl acetate
  9. washthe organic layer was washed with water until it
  10. customThe solvent was then dried under reduced pressure
  11. customThe residue was purified

출처 및 근거

ORD 기록
ord-a7fe4827bf244e3ca18040ef561605d5
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07604683B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트