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

Acetic Acid → 1-(1-Ethyl-4-hydroxy-5-methyl-1H-pyrazol-3-yl)ethanone

HRID 1880330
노트
인쇄 미리보기

반응식

HRID 1880330 반응식
[CH3:1][C:2]([CH:4]=O)=[O:3].[C:6]([OH:11])(=O)[C:7](O)=O.[CH2:12]([NH:14][NH2:15])[CH3:13].[C:16](O)(=O)C>O>[CH2:12]([N:14]1[C:7]([CH3:16])=[C:6]([OH:11])[C:4]([C:2](=[O:3])[CH3:1])=[N:15]1)[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 880MethylglyoxalHCID 96181Hydrazine, ethyl-, ethanedioate (1:1)

생성물 1

HCID 534402521-(1-Ethyl-4-hydroxy-5-methyl-1H-pyrazol-3-yl)ethanone수율 56%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

An aqueous solution of methyl glyoxal (pyruvaldehyde) (40%, 6.5 mL, 40 mmol) was added to a solution of ethylhydrazine oxalate (1 g, 6.7 mmol) and acetic acid (0.57 mL, 10 mmol) in water (11 mL), and the resulting mixture was heated at reflux for 3 hours. The reaction mixture was cooled to room temperature and extracted with EtOAc (3×). The combined organic layers were dried, filtered, and concentrated under reduced pressure. The crude product was purified by flash chromatography (silica gel) eluting with a gradient of heptane to heptane:ethyl acetate (80:20) to give 622 mg (56%) of 1-(1-ethyl-4-hydroxy-5-methyl-1H-pyrazol-3-yl)ethanone as a white solid.

후처리

  1. temperaturethe resulting mixture was heated
  2. temperatureat reflux for 3 hours
  3. extractionextracted with EtOAc (3×)
  4. customThe combined organic layers were dried
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe crude product was purified by flash chromatography (silica gel)
  8. washeluting with a gradient of heptane to heptane:ethyl acetate (80:20)

출처 및 근거

ORD 기록
ord-1a8b0048c53c4b208fb121e42315d3de
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318762B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트