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

Water → 2-Hydroxyquinoline

HRID 1586082
노트
인쇄 미리보기

반응식

HRID 1586082 반응식
N[C:2]1[CH:11]=[C:10]2[C:5]([C:6](OC)=[C:7](OC(=O)C)[C:8](=[O:13])[N:9]2C)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].CI.O>CN(C=O)C>[NH:9]1[C:10]2[C:5](=[CH:4][CH:3]=[CH:2][CH:11]=2)[CH:6]=[CH:7][C:8]1=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 154351697-Amino-4-methoxy-1-methyl-2-oxo-1,2-dihydroquinolin-3-yl acetate

생성물 1

HCID 60382-Hydroxyquinoline수율 86.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a mixture of 0.95 g of 7-amino-3-acetoxy-4-methoxy-1-methyl-2(1H)-quinolinone (3.6 mmol) in 20 ml of DMF were added 0.55 g of potassium carbonate (4.0 mmol) and 0.56 g of methyl iodide (4.0 mmol) and stirred at room temperature for 1 hour. The reaction mixture was added to water and extracted with toluene, the organic layer was concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (hexane/ethyl acetate=1/1 as an eluent) gave 0.45 g of the title compound (9). (yield=45%)

후처리

  1. extractionextracted with toluene
  2. concentrationthe organic layer was concentrated under reduced pressure
  3. customPurification of the residue by column chromatography on silica gel (hexane/ethyl acetate=1/1 as an eluent)

출처 및 근거

ORD 기록
ord-8b24bacb03204ddc82e1be7e4194bdb9
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05942521

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트