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

Hydrochloric Acid → Quinolin-4(3H)-one

HRID 635518
노트
인쇄 미리보기

반응식

HRID 635518 반응식
[NH2:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9]C=CC=1)=O.C[O-].[Na+].C([O:16][CH2:17][CH3:18])=O.Cl.O1CCO[CH2:22][CH2:21]1>O>[N:1]1[C:2]2[C:18](=[CH:9][CH:10]=[CH:5][CH:3]=2)[C:17](=[O:16])[CH2:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 8025Ethyl formateHCID 11952PhenacylamineHCID 312751,4-DioxaneHCID 10942334Sodium Methoxide

생성물 1

HCID 14418036Quinolin-4(3H)-one수율 60%

시약·촉매·용매 1

HCID 962
Water
용매

실험 절차

2-Aminoacetophenone (7.0 g, 52 mmol) was added to and dissolved in 1,4-dioxane (100 ml). To the solution obtained was added sodium methoxide (8.4 g, 156 mmol), and the mixture was stirred at room temperature for 30 minutes. Ethyl formate (21 ml, 261 mmol) was then added, and the mixture was stirred at room temperature for an additional 125 minutes. After adding water (5 ml) to the reaction solution, and stirring for 10 minutes, 10% hydrochloric acid was added to the mixture for neutralization. The reaction solution was then concentrated under reduced pressure. The residue was suspended in chloroform (100 ml), collected by filtration, washed with chloroform (100 ml), and then purified by silica gel column chromatography to give 4.5 g of the desired compound (yield 60%).

후처리

  1. customTo the solution obtained
  2. stirringthe mixture was stirred at room temperature for an additional 125 minutes
  3. stirringstirring for 10 minutes
  4. concentrationThe reaction solution was then concentrated under reduced pressure
  5. filtrationcollected by filtration
  6. washwashed with chloroform (100 ml)
  7. custompurified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-d682050077764efa8dbf3d64c8c8bfb9
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06187926B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트