반응식
[F:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([CH2:15][CH3:16])([OH:14])[C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.[CH2:19]([N:22]=[C:23]=[O:24])[CH2:20][CH3:21].C(=O)([O-])[O-].[K+].[K+].C(#N)C>C(O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([CH2:15][CH3:16])([OH:14])[C:7]2[CH:12]=[CH:11][C:10]([O:13][C:23](=[O:24])[NH:22][CH2:19][CH2:20][CH3:21])=[CH:9][CH:8]=2)=[CH:17][CH:18]=1참가 물질
실험 절차
12.3 g. of 4-fluoro-4'-hydroxy-α-ethyl-benzhydrol, 4.68 g. of n-propyl-isocyanate and 0.7 g. of anhydrous, powdered potassium carbonate in 61 ml. of acetonitrile containing 15 μlit. of a 50% aqueous ethanol solution are refluxed under stirring. When the reaction is complete, the reaction mixture is cooled to room temperature, potassium carbonate is filtered off and acetonitrile is distilled off under reduced pressure. The residue is dissolved in benzene, the benzene solution is shaken with a 5% aqueous sodium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and benzene is distilled off under reduced pressure. Crystallization of the residue from a mixture of ethyl acetate and n-hexane yields 13.6 g. of the desired compound, melting at 107° to 108° C.
후처리
- filtrationpotassium carbonate is filtered off
- distillationacetonitrile is distilled off under reduced pressure
- dissolutionThe residue is dissolved in benzene
- stirringthe benzene solution is shaken with a 5% aqueous sodium hydroxide solution
- washwashed to neutral with water
- dry with materialThe organic phase is dried over anhydrous magnesium sulfate
- filtrationfiltered
- distillationbenzene is distilled off under reduced pressure
- customCrystallization of the residue
- additionfrom a mixture of ethyl acetate and n-hexane
- customyields 13.6 g
출처 및 근거
- ORD 기록
- ord-4d11fe74511e4c3eb171abfda8490584
- 출처 데이터셋
- uspto-grants-1986_01
- 특허 번호
- US04564630
연결된 노트
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