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

Ethanol → 3,4-Dihydroxy-1-methylquinolin-2(1H)-one

HRID 1612761
노트
인쇄 미리보기

반응식

HRID 1612761 반응식
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:12])[C:4](=NO)[C:3]1=[O:15].[H][H].C([OH:20])C>[Pd].Cl>[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([OH:12])=[C:4]([OH:20])[C:3]1=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 702EthanolHCID 178418361HCID 178418361, 화합물HCID 178481576HCID 178481576, 화합물2회

생성물 1

HCID 546957683,4-Dihydroxy-1-methylquinolin-2(1H)-one

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 313Hydrochloric Acid용매

실험 절차

A suspension of 1-methyl-3-oximino-quinolin-2,4(1H)-dione (1.7 gm, Formula 1.02, Example 1) and 10% palladium on charcoal (0.5 gm) in a mixture of ethanol (90 ml) and 2N hydrochloric acid (40 ml) was hydrogenated at atmospheric conditions. After 2.5 hrs no further uptake of hydrogen (510 ml) was observed. The reaction mixture was filtered and the solid cake was extracted with hot glacial acetic acid (2×100 ml). The combined filtrates were evaporated under reduced pressure and the produce was crystallized from acetic acid/water to give the title compound (1.6 gm). That the expected product was obtained was confirmed by the spectral data: MS (FAB): m/e 192 (M.+ +1); NMR (DMSO): δ3.66 (s, 3H, CH3 --N), 8.79 (s, 1H, OH), 10.16 (s, 1H, OH) ppm.

후처리

  1. filtrationThe reaction mixture was filtered
  2. extractionthe solid cake was extracted with hot glacial acetic acid (2×100 ml)
  3. customThe combined filtrates were evaporated under reduced pressure
  4. customthe produce was crystallized from acetic acid/water

출처 및 근거

ORD 기록
ord-bc801b02f3114cc9a73aa81d76976dc7
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05190956

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트