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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867243Generated: October 25, 2026

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

https://huagongshe.com/reaction/867243

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 two hours. The reaction mixture was rendered slightly alkaline by the addition of 50 percent aqueous sodium hydroxide 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 numberUS04103092
Source datasetuspto-grants-1978_07
ORD IDord-88073dd9643d46da9a38ba0e31b4a63c
Source noteuspto-grants-1978_07