反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- -78 °C
PROCEDURE
实验过程
A solution of sec-butyl lithium in hexane (1.1M, 67.38 ml) was added to a solution of 4-bromobiphenyl (14.38 g) in dry tetrahydrofuran (128 ml) over a period of 1.5 hours under an atmosphere of argon at -78° C. The reaction mixture was stirred for 30 minutes at -78° C. A solution of 3-cyanoquinuclidine (5.6 g) in dry tetrahydrofuran was added to the reaction mixture whilst maintaining the temperature at -78° C. The reaction mixture was stirred for a further period of 16 hours during which period the reaction mixture was allowed to warm to ambient temperature. 2M aqueous hydrogen chloride solution (50 ml) was added to the reaction mixture and the mixture was stirred for 1 hour. The aqueous phase was separated, washed with diethyl ether, basified with dilute aqueous sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate extract was dried (MgSO4) and evaporated to give a residue which was purified by flash column chromatography on silica gel using a 95:5 (v/v) mixture of methanol/ammonia (density 0.88 g/cm3) as eluant. The residue was dissolved in ethanol and acidified with a saturated solution of ethanolic hydrogen chloride. The mixture was evaporated to dryness and hexane was added to give 3-(4-phenylbenzoyl)quinuclidine hydrogen chloride as a solid (970 mg), m.p. 255.6° C.; microanalysis, found: C, 71.4; H, 6.7; N, 4.4; Cl, 9.8%; C20H21NO. HCl 1/2 H2O. requires: C, 71.34; H, 6.8; N, 4.2; Cl, 10.5%; NMR (CDCl3): 1.7-1.85 (2H, m), 2.0-2.2 (2H, m), 2.2-2.45 (1H, m), 2.45-2.6 (1H, m), 3.2-3.5 (3H, m), 3.5-3.7 (2H, m), 3.9-4.2 (2H, m), 7.35-7.55 (3H, m), 7.55-7.65 (2H, m), 7.65-7.75 (2H, d), 8.0-8.1 (2H, d) and 12.26 (1H, s).
WORKUP
后处理
- temperaturewhilst maintaining the temperature at -78° C
- stirringThe reaction mixture was stirred for a further period of 16 hours during which period the reaction mixture
- temperatureto warm to ambient temperature
- stirringthe mixture was stirred for 1 hour
- customThe aqueous phase was separated
- washwashed with diethyl ether
- extractionextracted with ethyl acetate
- extractionThe ethyl acetate extract
- dry with materialwas dried (MgSO4)
- customevaporated
- customto give a residue which
- customwas purified by flash column chromatography on silica gel using
- additiona 95:5 (v/v) mixture of methanol/ammonia (density 0.88 g/cm3) as eluant
- dissolutionThe residue was dissolved in ethanol
- customThe mixture was evaporated to dryness and hexane
- additionwas added