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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199494Generated: November 1, 2026

Triethylamine → 1-[4-[(Methylsulfonyl)amino]benzoyl]aziridine

https://huagongshe.com/reaction/1199494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAziridineHCID 9033—
Reactant4-[(Methylsulfonyl)amino]benzoyl chlorideHCID 11791119—
SolventDichloromethaneHCID 6344—
Product1-[4-[(Methylsulfonyl)amino]benzoyl]aziridineHCID 14773549—

Reaction Conditions

Temperature0 °C

Reaction Steps

13.0 g (55.6 mmol) of 4-[(methylsulfonyl)amino]benzoyl chloride is suspended in 150 mL of methylene chloride and cooled to about 0° C. 2.40 g (55.7 mmol) of aziridine and 7.75 mL (55.6 mmol) of triethylamine are added and the reaction allowed to warm to room temperature and stir for 2 hours. After 2 hours, the solution is washed with 100 mL of saturated aqueous sodium chloride and placed in the freezer. After 18 hours, the resulting white precipitate is filtered, washed with 50 mL of ether and dried to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900841
Source datasetuspto-grants-1990_02
ORD IDord-cab3e4b782604ee880c0f55346d0d0a3
Source noteuspto-grants-1990_02