Acetic Acid → HCID 86755685, 화합물
반응식
[H-].[Na+].[C:3]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])=[CH:14][CH:13]=2)=[CH:8][CH:7]=1)(=O)[CH3:4].[C:25]([OH:28])(=[O:27])[CH3:26].O1CC[CH2:31][CH2:30]1>>[CH2:18]([C:15]1[CH:16]=[CH:17][C:12]([C:9]2[CH:10]=[CH:11][C:6](/[C:3](/[CH3:4])=[CH:26]/[C:25]([O:28][CH2:30][CH3:31])=[O:27])=[CH:7][CH:8]=2)=[CH:13][CH:14]=1)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]참가 물질
실험 절차
To a suspension of sodium hydride (60% in oil, 0.37 g) in tetrahydrofuran (40 ml) was added by portions 4-acetyl-4′-n-heptylbiphenyl (2.50 g) at ambient temperature. After stirring at ambient temperature for 1 hours, to the solution was added triethyl phosphonoacetate (1.9 ml) and the mixture was heated to reflux for 5 hours. After cooling to ambient temperature, to the mixture was added acetic acid (0.53 ml) and evaporated. The residue was taken up into a mixture of water and ethyl acetate. The separated organic layer was washed with brine, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (200 ml) eluting with mixture of n-hexane and diisopropyl ether (99:1-20:1, V/V) to give Ethyl (E)-3-[4-(4-heptylphenyl)phenyl]-2-butenoate (2.19 g).
후처리
- temperaturethe mixture was heated
- temperatureto reflux for 5 hours
- temperatureAfter cooling to ambient temperature, to the mixture
- customevaporated
- additionThe residue was taken up into a mixture of water and ethyl acetate
- washThe separated organic layer was washed with brine
- dry with materialdried over magnesium sulfate
- customevaporated
- customThe residue was chromatographed on silica gel (200 ml)
- washeluting with mixture of n-hexane and diisopropyl ether (99:1-20:1, V/V)
출처 및 근거
- ORD 기록
- ord-a2517018ed9c4fb19f04eb85ba89bc1c
- 출처 데이터셋
- uspto-grants-2001_07
- 특허 번호
- US06265536B1
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