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
PROCEDURE
实验过程
To a stirred solution of 8.0 g. (0.048 mole) of α-(2-aminomethyl-1,4-cyclohexadienyl)acetic acid and 3.8 g. (0.096 mole) of NaOH in 150 ml. of water was added a solution of 10.3 g. (0.072 mole) of t-butoxycarbonylazide in 80 ml. of THF and the mixture was stirred for 18 hours at room temperature. The THF was removed under reduced pressure and the residual solution was washed with ether (2 × 100 ml.), acidified with 6 N HCl and extracted with ether (3 × 100 ml.). The combined extracts were washed with water (2 × 100 ml.) and a saturated NaCl solution (100 ml.), dried with Na2SO4 and evaporated to dryness. The oily residue was triturated with n-hexane to give 10.5 g. (82%) of colorless powder melting at 113° C.
WORKUP
后处理
- customThe THF was removed under reduced pressure
- washthe residual solution was washed with ether (2 × 100 ml.)
- extractionextracted with ether (3 × 100 ml.)
- washThe combined extracts were washed with water (2 × 100 ml.)
- dry with materiala saturated NaCl solution (100 ml.), dried with Na2SO4
- customevaporated to dryness
- customThe oily residue was triturated with n-hexane
- customto give 10.5 g