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
- 0 °C
PROCEDURE
实验过程
A stirred mixture of 1-(4-trifluoromethylbenzoyl)-2-chloro-4,6-dimethylbenzene (6.90 g, 22.1 mmol), N-bromosuccinimide (3.94 g, 22.1 mmol), and dibenzoyl peroxide (224 mg, 0.925 mmol) in dry carbon tetrachloride (180 ml) was refluxed 44 hours. Additional N-bromosuccinimide (1.97 g, 11.1 mmol) was added and the mixture was refluxed 24 hours. The mixture was cooled to 0° C., filtered, and washed with carbon tetrachloride. The combined filtrate and washes were evaporated to dryness under vacuum, and the residue was dissolved in dichloromethane (135 ml), treated with tetramethylguanidinium azide (7.25 g, 45.8 mmol), and stirred 40 minutes at ambient temperature. Solvent was removed under vacuum and the residue was stirred with diethyl ether (180 ml). The mixture was filtered and the precipitate was washed with diethyl ether. The combined filtrate and washes were washed twice with water and once with brine, dried over anhydrous magnesium sulfate, and evaporated to dryness under vacuum. The residue was dissolved in hexane (300 ml) and decanted, and the residual gum was washed with hexane. The combined hexane layers were evaporated to dryness under vacuum. The residue was chromatographed on silica gel (500 g) eluted with 93:7 (v/v) hexane-ethyl acetate using a preparative high-performance liquid chromatograph to provide 1.71 g (22%) oily 4-(4-trifluoromethylbenzoyl)-3-chloro-5-methylbenzyl azide (A), 1.30 g (17%) 2-(4-trifluoromethylbenzoyl)-3-chloro-5-methylbenzyl azide (B), and 0.48 g of a mixture of A and B.
WORKUP
后处理
- temperaturewas refluxed 44 hours
- temperaturethe mixture was refluxed 24 hours
- filtrationfiltered
- washwashed with carbon tetrachloride
- customThe combined filtrate and washes were evaporated to dryness under vacuum
- dissolutionthe residue was dissolved in dichloromethane (135 ml)
- customSolvent was removed under vacuum
- stirringthe residue was stirred with diethyl ether (180 ml)
- filtrationThe mixture was filtered
- washthe precipitate was washed with diethyl ether
- washThe combined filtrate and washes were washed twice with water and once with brine
- dry with materialdried over anhydrous magnesium sulfate
- customevaporated to dryness under vacuum
- dissolutionThe residue was dissolved in hexane (300 ml)
- customdecanted
- washthe residual gum was washed with hexane
- customThe combined hexane layers were evaporated to dryness under vacuum
- customThe residue was chromatographed on silica gel (500 g)
- washeluted with 93:7 (v/v) hexane-ethyl acetate using a preparative high-performance liquid chromatograph