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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462149Generated: October 25, 2026

Hydrochloric Acid → N,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-aminopropylammonium chloride

https://huagongshe.com/reaction/462149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantN,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-formamidopropylammonium chlorideHCID 86733006—
SolventWaterHCID 962—
ProductN,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-aminopropylammonium chlorideHCID 86733010—

Reaction Steps

A solution of 10.0 parts of N,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-formamidopropylammonium chloride in 100 parts of water containing 6.0 parts of concentrated hydrochloric acid was heated for about 2 hours. The reaction mixture was rendered slightly alkaline by the addition of 50 percent aqueous sodium hyroxide and stored in the refrigerator for 2 days. The reaction mixture was then filtered to remove a small amount of solid and the filtrate was acidified with 48 parts of concentrated hydrochloric acid. Acetone was slowly added to the acidified filtrate until precipitation started. When precipitation of the product was complete, the solid was collected on a filter, washed with acetone, and dried at 75° C. to obtain 8.2 parts of N,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-aminopropylammonium chloride as the mono-hydrochloride salt, a white solid which melted at 244°-245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065500
Source datasetuspto-grants-1977_12
ORD IDord-88de4f92951449fa9e5e9af55a8c96d1
Source noteuspto-grants-1977_12