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, under nitrogen, of α-chloro-2-bromobenzaldehyde phenylsulfonylhydrazone (271.1 g; 720 mmol) in tetrahydrofuran (THF; 2 L), was added dropwise N-methylpiperazine (159.7 g; 1600 mmol). The reaction was stirred at ambient temperature for three hours, and then permitted to stand at ambient temperature of 16 hours. The reaction was chilled in an ice bath, and then filtered to remove the piperazine hydrochloride that was formed. The filtrate was concentrated to yield a brown gum. The gum was triturated with hot acetonitrile, the mixture was cooled in an ice bath, and when cold, was filtered to remove unwanted side product. The filtrate was then concentrated to afford 392.9 g of a brown gum of crude 1-[[(phenylsulfon-yl)hydrazono]-(2-bromophenyl)methyl]-4-methylpiperazine.
WORKUP
后处理
- waitto stand at ambient temperature of 16 hours
- temperatureThe reaction was chilled in an ice bath
- filtrationfiltered
- customto remove the piperazine hydrochloride that
- customwas formed
- concentrationThe filtrate was concentrated
- customto yield a brown gum
- customThe gum was triturated with hot acetonitrile
- temperaturethe mixture was cooled in an ice bath
- filtrationwhen cold, was filtered
- customto remove unwanted side product
- concentrationThe filtrate was then concentrated