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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437646Generated: October 29, 2026

Aziridine → HCID 21428907, compound

https://huagongshe.com/reaction/437646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAziridineHCID 9033—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Chloro-2-methoxy-4-nitrobenzoyl chlorideHCID 21428911—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 21428907HCID 21428907—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 230 parts of a solution of aziridine in water 0.875M are added 15 parts of sodium hydrogen carbonate while cooling at 0° C. Then there is added dropwise, during a 45 minutes-period, a solution of 42.5 parts of 5-chloro-2-methoxy-4-nitrobenzoyl chloride in 150 parts of trichloromethane at 0° C and while stirring vigorously. The mixture is diluted with about 150 parts of trichloromethane and the whole is stirred for 45 minutes without cooling. The reaction mixture is alkalized to pH 8 with a diluted sodium hydroxide solution. The product is extracted three times with trichloromethane. The combined extracts are washed three times with water, dried, filtered and evaporated, yielding 40 parts of 1-(5-chloro-2-methoxy-4-nitrobenzoyl)aziridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-79bcea7f1d884e8790e68d820613a4a5
Source noteuspto-grants-1977_06