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2-Hydroxy-4-oxo-4-phenylbutanoic acid → 4,5-dihydro-4-hydroxy-2-(2-hydroxybutyl)-6-phenylpyridazin-3(2H)-one

HRID 1447726
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HRID 1447726 반응식
[C:1]([CH2:9][CH:10]([OH:14])[C:11]([OH:13])=O)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:15]([CH2:17][CH:18]([OH:21])[CH2:19][CH3:20])[NH2:16]>C(O)CCC>[OH:14][CH:10]1[CH2:9][C:1]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[N:16][N:15]([CH2:17][CH:18]([OH:21])[CH2:19][CH3:20])[C:11]1=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5166992-Hydroxy-4-oxo-4-phenylbutanoic acidHCID 41131272-Hydroxybutylhydrazine

생성물 1

HCID 203842894,5-dihydro-4-hydroxy-2-(2-hydroxybutyl)-6-phenylpyridazin-3(2H)-one

시약·촉매·용매 1

HCID 2631-Butanol용매

반응 조건

온도
120 °C

실험 절차

A mixture of 3.5 grams (18 mmol) of 3-benzoyl-2-hydroxy-propionic acid and 1.9 grams (18 mmol) of 1-hydrazino-2-butanol in 40 ml of n-butanol is refluxed under nitrogen at 120° C. for 18 hours. After evaporation of the solvent, the product is partitioned between ether and water. The ether layer is washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate, and evaporated. The resulting residue is dissolved in 2% ethanol-chloroform and filtered through 200 grams of silica gel yielding after evaporation 4,5-dihydro-4-hydroxy-2-(2-hydroxybutyl)-6-phenylpyridazin-3(2H)-one, m.p. 92°-94° C.

후처리

  1. customAfter evaporation of the solvent
  2. customthe product is partitioned between ether and water
  3. washThe ether layer is washed with aqueous sodium bicarbonate and brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. dissolutionThe resulting residue is dissolved in 2% ethanol-chloroform
  7. filtrationfiltered through 200 grams of silica gel yielding
  8. customafter evaporation 4,5-dihydro-4-hydroxy-2-(2-hydroxybutyl)-6-phenylpyridazin-3(2H)-one, m.p. 92°-94° C.

출처 및 근거

ORD 기록
ord-795c59f2dd2e4ef897c40618018f9087
출처 데이터셋
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04177273

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