Tetrahydrofuran → HCID 67794827、化合物
反応式
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]2[C:6](=[CH2:15])[C:7]3[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=3[CH:9]=[CH:10][C:4]=2[CH:3]=1.C12BC(CCC1)CCC2.[O:27]1CCCC1>>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]2[CH:6]([CH2:15][OH:27])[C:7]3[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=3[CH:9]=[CH:10][C:4]=2[CH:3]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a solution of 2-chloro-5-methylene-dibenzo[a,d]cycloheptene (8.3 g) in dry tetrahydrofuran (30 ml). under an inert atmosphere, was added 9-borabicyclo [3.3.1]nonane (71 ml of a 0.5 molar solution in tetrahydrofuran) at ambient temperature and the reaction mixture was then refluxed for 3 h. After cooling. the reaction was quenched by the slow addition of 2N sodium hydroxide solution (180 ml) and 30% hydrogen peroxide (36 ml). After stirring vigorously at 0° C. for 45 minutes the reaction mixture was allowed to warm to room temperature over a 2 h period then extracted into diethyl ether (3×250 ml). The combined organic layers were washed with brine (1×150 ml), dried (Na2SO4), filtered and concentrated in vacuo to leave a residue which was purified by chromatography on flash silica with 40% ethyl acetate in hexane as eluent to give the title compound (8.1 g) as a colourless oil. δ (360 MHz, CDCl3) 3.80 (2H. d, J=7.9 Hz CH--CH2OH), 4.18 (1H, t, J= 7.9 Hz, CH--CH2OH), 6.76 (1H, d, J=11.9 Hz, CHA =CHB) 6.89 (1H, d, J=11.9 Hz, CHA =CHB), 7.24-7.38 (7H, m, ArH); m/e 258 and 256 (M+)