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HRID 421522作成日:2026年10月27日

4-Toluenesulfonyl chloride → N,N-bis(2-chloroethyl)-p-toluenesulphonamide

https://huagongshe.com/reaction/421522

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
反応物Bis(2-chloroethyl)amine hydrochlorideHCID 522769—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TetrahydrofuranHCID 8028—
生成物N,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 9603980.1%

反応手順

To a suspension of bis(2-chloroethyl)amine hydrochloride (4.68 g, 26.2 mmol) in dry THF (50 mL) was added Et3N (18.3 mL, 131 mmol) at 0° C. and the mixture was stirred for 15 min. p-Toluenesulfonyl chloride (5.00 g, 26.25 mmol) and DMAP (a spatula pinch) were added. The reaction mixture was allowed to warm to room temperature and was stirred overnight. When TLC analysis showed complete conversion, the mixture was filtered to remove the Et3N.HCl and extracted with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash column chromatography to afford N,N-bis(2′-chloroethyl)-4-methylbenzenesulfonamide (6.22 g, 80% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101238B2
出典データセットuspto-grants-2012_01
ORD IDord-6c4eed1389624149a76331714ac9fde2
出典メモuspto-grants-2012_01