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
To a solution of (1-carbamoyl-2-isobutyl-cyclopropylmethyl)-carbamic acid tert-butyl ester (5.8 g, 21.5 mmol) in dry DMF (100 mL) was added cyanuric chloride (5.5 g, 30.1 mmol). The reaction mixture was stirred at 0° C. for 30 minutes and was poured into cold 0.5N NaOH (200 mL). The aqueous phase was extracted with EtOAc (2×150 mL) and the combined organic layer was washed with water and brine and dried over Na2SO4. Removal of excess of solvent, followed by purification of the residue by flash column chromatography using hexanes/EtOAc (9:1) as eluent gave 4.9 g (91%) of (1-cyano-2-isobutyl-cyclopropylmethyl)-carbamic acid tert-butyl ester as a colorless foam: 1H NMR (300 MHz, CDCl3) δ 0.86 (m, 1H), 0.94 (d, J=4.0 Hz, 3H), 0.96 (d, J=4.0 Hz, 3H), 1.56 (m, 1H), 1.37-1.56 (m, 12H), 1.71 (m, 1H), 3.32 (d, J=6.1 Hz, 2H), 5.26 (s, 1H); 13C (75 MHz, CDCl3) δ 14.5, 18.8, 21.9, 22.2, 24.4, 28.0, 28.1, 36.3, 40.4, 79.3, 122.9, 155.4; MS (APCI) m/z 253 [M+H]+.
WORKUP
后处理
- extractionThe aqueous phase was extracted with EtOAc (2×150 mL)
- washthe combined organic layer was washed with water and brine
- dry with materialdried over Na2SO4
- customRemoval of excess of solvent
- customfollowed by purification of the residue by flash column chromatography