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2-Oxobutanoic Acid → HCID 12979375, 화합물

HRID 1362426
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HRID 1362426 반응식
[C:1]1([CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH:7]N.O=[C:11]([CH2:15][CH3:16])[C:12]([OH:14])=[O:13].[CH2:17](O)[CH3:18]>>[CH3:16][C:15]1[C:3]2[C:2](=[C:1]([CH3:9])[CH:6]=[CH:5][CH:4]=2)[NH:7][C:11]=1[C:12]([O:14][CH2:17][CH3:18])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 582-Oxobutanoic AcidHCID 702Ethanol2회HCID 68256o-Tolylhydrazine

생성물 1

HCID 12979375HCID 12979375, 화합물수율 27%

반응 조건

온도
50 °C

실험 절차

A suspension of 1-o-tolylhydrazine (3.8 g, 30.9 mmol) in ethanol was warmed to 50° C. A solution of α-ketobutyric acid (3.16 g, 30.9 mmol) in ethanol was added and the mixture stirred at rt overnight. Hydrogen chloride was bubbled through the solution for 30 min and the mixture heated at reflux for 2 h then evaporated in vacuo. The crude reaction was chromatographed over silica gel eluting with ethyl acetate/hexane (5%) to afford the title compound (1.84 g, 27%). 1H NMR (400 MHz, CDCl3) δ 8.55 (s, 1H), 7.50 (d, J=7.8 Hz, 1H), 7.09 (d, J=6.9 Hz, 1H), 7.03 (t, J=7.6 Hz, 1H), 4.41 (q, J=7.1 Hz, 2H), 2.59 (s, 3H), 2.48 (s, 3H), 1.44 (t, J=7.2 Hz, 3H).

후처리

  1. customHydrogen chloride was bubbled through the solution for 30 min
  2. temperaturethe mixture heated
  3. temperatureat reflux for 2 h
  4. customthen evaporated in vacuo
  5. customThe crude reaction
  6. customwas chromatographed over silica gel eluting with ethyl acetate/hexane (5%)

출처 및 근거

ORD 기록
ord-293a50948ce1460b9b58ad17aae28cf1
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879872B2

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