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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202174Generated: October 30, 2026

Triethylamine → n,n-Bis(2-chloroethyl)methanesulfonamide

https://huagongshe.com/reaction/2202174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBis(2-chloroethylamine) hydrochlorideHCID 86583559—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Productn,n-Bis(2-chloroethyl)methanesulfonamideHCID 24509282.7%

Reaction Steps

14.3 ml (185 mmol) of methanesulfonyl chloride are added slowly to a solution of 15 g (84 mmol) of commercial bis(2-chloroethylamine) hydrochloride and 26 ml (185 mmol) of triethylamine in 200 ml of dichloromethane and 70 ml of tetrahydrofuran previously stirred for 15 min and then filtered in order to remove the triethylammonium chloride. The reaction medium is then stirred at ambient temperature for 18 h, extracted with dichloromethane, and washed with water. The organic phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is washed with diisopropyl ether, filtered and then dried under vacuum. 15.3 g (82%) of N,N-bis-(2-chloroethyl)methanesulfonamide are obtained in the form of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-a07a8270bc77483aa364a1c750ce4437
Source noteuspto-grants-2016_06