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 solution of 15.0 g (0.05 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methylnaphth[2,1-f][1,4]-oxazepine-5(4H)-thione in 50 ml of absolute ethanol was added 10 g of a 40% aqueous solution of dimethylamine. The resulting solution was heated in a steel bomb at 100° C. for 40 hr and concentrated under reduced pressure. The residue was partitioned between 15% aqueous sodium hydroxide and chloroform. The chloroform layer was evaporated and the residue partitioned between 3N hydrochloric acid and chloroform. The aqueous layer was made alkaline with 50% sodium hydroxide and extracted with chloroform. The chloroform extract was concentrated and the residue dissolved in isopropyl alcohol. Ethereal hydrogen chloride was added. Recrystallization of the precipitate from isopropyl alcohol/water gave 3.0 g (20%) of the product, m.p. 238°-240° C.
WORKUP
后处理
- concentrationconcentrated under reduced pressure
- customThe residue was partitioned between 15% aqueous sodium hydroxide and chloroform
- customThe chloroform layer was evaporated
- customthe residue partitioned between 3N hydrochloric acid and chloroform
- extractionextracted with chloroform
- extractionThe chloroform extract
- concentrationwas concentrated
- dissolutionthe residue dissolved in isopropyl alcohol
- additionEthereal hydrogen chloride was added
- customRecrystallization of the precipitate from isopropyl alcohol/water