Sodium Bicarbonate → HCID 178511233、化合物

反応式

[Cl-].[F:2][C:3]1[CH:4]=[C:5]([C:10]2[CH:15]=[CH:14][C:13]([CH2:16][P+](C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)=[CH:12][N:11]=2)[CH:6]=[CH:7][C:8]=1[F:9].[CH:36]([C@H:38]1[CH2:43][CH2:42][C@H:41]([C:44]#[N:45])[CH2:40][CH2:39]1)=O.C(=O)([O-])O.[Na+]>C(OCC)C>[F:2][C:3]1[CH:4]=[C:5]([C:10]2[CH:15]=[CH:14][C:13]([CH:16]=[CH:36][C@H:38]3[CH2:43][CH2:42][C@H:41]([C:44]#[N:45])[CH2:40][CH2:39]3)=[CH:12][N:11]=2)[CH:6]=[CH:7][C:8]=1[F:9]

参加物

実験手順

A suspension of 12.05 g of [2-(3,4-difluorophenyl)-5-pyridyl]methyltriphenylphosphonium chloride in 70 ml of diethyl ether is treated with 2.67 g of potassium tert.-butylate in a nitrogen atmosphere. The dark yellow suspension is stirred at room temperature for a further 30 minutes. A solution of 2.74 g of -trans-4-formylcyclohexanecarbonitrile in 30 ml of diethyl ether is then added dropwise at 0° C. The reaction mixture is stirred at 0° C. for a further 1 hour, then stirred with 40 ml of 1N sodium hydrogen carbonate solution and diluted with diethyl ether. The organic phase is separated, washed neutral with water, dried over sodium sulphate and concentrated. The residue is chromatographed on silica gel with hexane/ethyl acetate 3:1 (v/v). There is obtained trans-4-[2-[2-(3,4-difluorophenyl)-5-pyridyl]vinyl]cyclohexanecarbonitrile.