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
1.1 ml of acetic anhydride (12 mmol) are added to a mixture of 2.8 g of Z-Gln-OH (10 mmol), 5.2 g of triphenylmethanol (20 mmol) in 30 ml of acetic acid, and the mixture is stirred at 50° for 15 minutes. Then 0.05 ml of conc. sulfuric acid (about 1 mmol) is added, resulting in a clear yellow solution after a few minutes. After 2 hours, the solution is added dropwise to 500 ml of water, while stirring and cooling in ice, and the precipitate is filtered off and thoroughly washed with water. The moist material is dissolved in ethyl acetate, the aqueous phase is separated off, and the organic phase is washed once with a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure to 20 g. Z-Gln(Trt)-OH is crystallized by addition of hexane in portions, m.p. 161°-162°.
WORKUP
后处理
- customresulting in a clear yellow solution after a few minutes
- waitAfter 2 hours
- stirringwhile stirring
- temperaturecooling in ice
- filtrationthe precipitate is filtered off
- washthoroughly washed with water
- dissolutionThe moist material is dissolved in ethyl acetate
- customthe aqueous phase is separated off
- washthe organic phase is washed once with a saturated aqueous sodium chloride solution
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure to 20 g
- customZ-Gln(Trt)-OH is crystallized by addition of hexane in portions, m.p. 161°-162°