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

Acetone → 8-Methoxy-6-nitro-3,4-dihydroquinolin-2(1H)-one

HRID 1649001
노트
인쇄 미리보기

반응식

HRID 1649001 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[C:12]([OH:14])[CH:13]=1)[NH:10][C:9](=[O:15])[CH2:8][CH2:7]2)([O-:3])=[O:2].[C:16](=O)([O-])[O-].[K+].[K+].CC(C)=O.S(OC)(OC)(=O)=O>O>[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[C:12]([O:14][CH3:16])[CH:13]=1)[NH:10][C:9](=[O:15])[CH2:8][CH2:7]2)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 130510728-Hydroxy-6-nitro-3,4-dihydroquinolin-2(1H)-one

생성물 1

HCID 130510718-Methoxy-6-nitro-3,4-dihydroquinolin-2(1H)-one수율 77%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

6-Nitro-8-hydroxy-3,4-dihydrocarbostyril (10 g) and potassium carbonate (13.3 g) were mixed with acetone (70 ml) and water (70 ml) and the mixture was refluxed with adding dropwise 12.1 g of dimethyl sulfate. After refluxing was continued for 4 hours, the reaction mixture was cooled, and crystals which precipitated were collected by filtration and washed with water to give 8.22 g of 6-nitro-8-methoxy-3,4-dihydrocarbostyril.

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureAfter refluxing
  3. temperaturethe reaction mixture was cooled
  4. customcrystals which precipitated
  5. filtrationwere collected by filtration
  6. washwashed with water

출처 및 근거

ORD 기록
ord-ce801d41c2ee4dc780258c800ebf7e7a
출처 데이터셋
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04414390

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트