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 1350 ml. of ethanol there was added 90 gm. of 2-chloroacetamido-5-chlorobenzophenone and 92.5 gm. of hexamethylenetetramine. Ammonia was bubbled through the resultant medium under a pressure. The resultant medium was heated to reflux. The resultant reaction medium was evaporated in vacuum to dryness. It was triturated then with 250 ml. of hot water twice on a steam bath. The aqueous phase was removed by decantation. The crystalline residue was heated for 30 minutes in 250 ml. of toluene on a steam bath and then cooled to room temperature. The crystals which formed were filtered, washed twice with 25 ml. of toluene and 25 ml. of petroleum ether and dried to constant weight yielding 7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one melting point 213°-215° C.
WORKUP
后处理
- customAmmonia was bubbled through the resultant medium under a pressure
- temperatureThe resultant medium was heated to reflux
- customThe resultant reaction medium
- customwas evaporated in vacuum to dryness
- customIt was triturated
- customThe aqueous phase was removed by decantation
- temperatureThe crystalline residue was heated for 30 minutes in 250 ml
- customThe crystals which formed
- filtrationwere filtered
- washwashed twice with 25 ml
- dry with materialof petroleum ether and dried to constant weight