Water → 4-Hydroxy-2-butynyl 4-Cyano-3,4-diphenylbutyrate

HRID 1446780

반응식

HRID 1446780 반응식
[C:1]([CH:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH:4]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:5][C:6](Cl)=[O:7])#[N:2].[CH2:21]([OH:26])[C:22]#[C:23][CH2:24][OH:25].N1C=CC=CC=1.O>C1C=CC=CC=1.C1COCC1>[C:1]([CH:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH:4]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:5][C:6]([O:25][CH2:24][C:23]#[C:22][CH2:21][OH:26])=[O:7])#[N:2]

참가 물질

7

실험 절차

A solution of 10.7 g (0.038 mol) of 4-cyano-3,4-diphenylbutyryl chloride in 30 ml of benzene was added over a 45 minute period to a stirred solution of 6.5 g (0.076 mol) of 2-butyn-1,4-diol and 3.4 ml of pyridine in 100 ml of THF at 0°. The reaction mixture was stirred for 24 hours at room temperature in a flask equipped with a Drierite tube. The solution was poured into 50 ml of water and the layers were separated. Two 60-ml ether extractions of the aqueous layer were combined with the THF layer, were washed twice with 100 ml of H2O, with 100 ml saturated aqueous sodium bicarbonate, and with 100 ml saturated aqueous sodium chloride and were stirred over MgSO4. The filtered solution was stripped and purified by column chromatography on silica gel (hexanes/methylene chloride) to give two fractions weighing 12.6 g (47%) having different isomer ratios as determined from the nmr spectra. The infrared and nmr spectra are in accord with the assigned structure.

후처리

  1. customequipped with a Drierite tube
  2. customthe layers were separated
  3. extractionTwo 60-ml ether extractions of the aqueous layer
  4. washwere washed twice with 100 ml of H2O, with 100 ml saturated aqueous sodium bicarbonate
  5. stirringwith 100 ml saturated aqueous sodium chloride and were stirred over MgSO4
  6. custompurified by column chromatography on silica gel (hexanes/methylene chloride)
  7. customto give two fractions

출처 및 근거

ORD 기록
ord-b80b9c9f86d44a07b5d78fe3d538f9a5
출처 데이터셋
uspto-grants-1982_02
특허 번호
US04313754

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