반응식
[F:1][C:2]([F:21])([F:20])[C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][CH:19]=1)[C:6]([CH2:15][CH3:16])([OH:14])[C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1.[CH2:22]([N:26]=[C:27]=[O:28])[CH2:23][CH2:24][CH3:25].C(N(CC)CC)C.[OH-].[K+]>C1C=CC=CC=1>[F:1][C:2]([F:20])([F:21])[C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][CH:19]=1)[C:6]([CH2:15][CH3:16])([OH:14])[C:7]1[CH:8]=[CH:9][C:10]([O:13][C:27](=[O:28])[NH:26][CH2:22][CH2:23][CH2:24][CH3:25])=[CH:11][CH:12]=1참가 물질
실험 절차
8.9 g. of 3-trifluoromethyl-4'-hydroxy-α-ethyl-benzhydrol, 3.3 g. of n-butyl-isocyanate and 0.06 ml. of triethyl amine in 45 ml. of dry benzene are heated up to 50° C. under stirring, and the reaction mixture is kept at the same temperature for one additional hour. The progress of the reaction is monitored by thin layer chromatography. When the reaction is complete, the mixture is cooled to room temperature, the benzene solution is shaken with a 5% aqueous potassium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and the solvent is distilled off under reduced pressure. The solid residue is crystallized from a mixture of ethyl acetate and n-hexane. 11.4 g. of the named compound are obtained, melting at 99° to 100° C.
후처리
- washwashed to neutral with water
- dry with materialThe organic phase is dried over anhydrous magnesium sulfate
- filtrationfiltered
- distillationthe solvent is distilled off under reduced pressure
- customThe solid residue is crystallized from a mixture of ethyl acetate and n-hexane
- customof the named compound are obtained
출처 및 근거
- ORD 기록
- ord-f076cec6be3d4570b8a05b9fb53c40d8
- 출처 데이터셋
- uspto-grants-1986_01
- 특허 번호
- US04564630
연결된 노트
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