Dimethylacetamide → 4-{4-[2-(4-Propyl-cyclohexyl)-ethenyl]-phenyl}cyclohexane carboxylic acid methyl ester
반응식
CN(C)C(=O)C.P([O-])([O-])([O-])=O.[K+].[K+].[K+].[CH3:15][O:16][C:17]([CH:19]1[CH2:24][CH2:23][CH:22]([C:25]2[CH:30]=[CH:29][C:28](Br)=[CH:27][CH:26]=2)[CH2:21][CH2:20]1)=[O:18].[CH2:32]([CH:35]1[CH2:40][CH2:39][CH:38]([CH:41]=[CH2:42])[CH2:37][CH2:36]1)[CH2:33][CH3:34]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[CH3:15][O:16][C:17]([CH:19]1[CH2:24][CH2:23][CH:22]([C:25]2[CH:30]=[CH:29][C:28]([CH:42]=[CH:41][CH:38]3[CH2:39][CH2:40][CH:35]([CH2:32][CH2:33][CH3:34])[CH2:36][CH2:37]3)=[CH:27][CH:26]=2)[CH2:21][CH2:20]1)=[O:18]참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
180 mL of N,N-dimethylacetamide (DMA) solution including 12.8 g (60.1 mmol) of potassium phosphate, 14.3 g (48 mmol) of 4-(4-bromophenyl)cyclohexanecarboxylic acid methyl ester produced in Example 1-1, and 6.09 g (40 mmol) of 1-propyl-4-vinylcyclohexane was poured to flask filled with Argon gas. Then, 0.17 g (catalytic amount) of palladium acetate was added to the flask and reacted in oil bath at 120° C. for 32 hours. After reaction, 100 mL of distilled water was added to the reaction mixture, extracted by ethyl acetate, and then the aqueous layer was extracted by chloroform. The organic layer was dried by Na2SO4, concentrated under reduced pressure, and then recrystallized from ethanol to obtain 8.8 g (60%) of 4-{4-[2-(4-propyl-cyclohexyl)-ethenyl]-phenyl}cyclohexane carboxylic acid methyl ester.
후처리
- additionwas poured to flask
- additionfilled with Argon gas
- customreacted in oil bath at 120° C. for 32 hours
- additionwas added to the reaction mixture
- extractionextracted by ethyl acetate
- extractionthe aqueous layer was extracted by chloroform
- dry with materialThe organic layer was dried by Na2SO4
- concentrationconcentrated under reduced pressure
- customrecrystallized from ethanol
출처 및 근거
- ORD 기록
- ord-34bf4b2efda845679bb6f9bbc22e9307
- 출처 데이터셋
- uspto-grants-2013_08
- 특허 번호
- US08512598B2
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