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
4-[[(2,6-Dichlorophenyl)carbonyl]amino]-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine methyl ester (1.86 g, 4.0 mmol) was treated with 4 N hydrochloric acid in dioxane (10 mL) at room temperature. After 5 minutes, the solids went into solution and the mixture was stirred for 1 h. Then, 25 mL of ethyl ether was added to precipitate the product. The solids were collected by filtration and washed with hexane. The resulting solid was very hydroscopic and became gummy. This material was dissolved in 50 mL of methanol and concentrated. After drying under high vacuum, 4-[[(2,6-dichlorophenyl)carbony]amino]-L-phenylalanine methyl ester hydrochloride salt. (1.64 g, 97%) was obtained as a light yellow solid: mp 158-161° C.
WORKUP
后处理
- customto precipitate the product
- filtrationThe solids were collected by filtration
- washwashed with hexane
- dissolutionThis material was dissolved in 50 mL of methanol
- concentrationconcentrated
- dry with materialAfter drying under high vacuum, 4-[[(2,6-dichlorophenyl)carbony]amino]-L-phenylalanine methyl ester hydrochloride salt
- custom(1.64 g, 97%) was obtained as a light yellow solid