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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418839Generated: October 29, 2026

Chlorobenzene → HCID 178512041, compound

https://huagongshe.com/reaction/1418839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantPyrrolidine-1-carboximidamideHCID 2794597—
Reactant3-Nitroanilinium chlorideHCID 12215133—
SolventWaterHCID 962—
ProductHCID 178512041HCID 178512041—

Reaction Steps

Samples of 3-nitroaniline hydrochloride, 15.5 g, and 1-pyrrolidinecarboximidamide, 9.6 g, were combined with 12 ml of chlorobenzene, and the mixture was warmed to reflux for three hours, and then allowed to cool. The resulting solid mass was taken up in 200 ml of hot water, and the chlorobenzene layer was separated. The aqueous layer was washed with 30 ml of chloroform and the combined organic layers were washed with 50 ml of water. The aqueous layers were combined, warmed, treated with charcoal and filtered hot. The filtrate was allowed to cool, and made strongly basic with 50% sodium hydroxide. This basic mixture was extracted with 200 ml of chloroform. The chloroform extract was concentrated on a steam bath to 150 ml, then diluted with hexanes to 300 ml, and stirred until yellow solids formed, giving 17 g of the N-(3-nitrophenyl)-1-pyrrolidinecarboximidamide, m.p. 117°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885985
Source datasetuspto-grants-1999_03
ORD IDord-8b837cfaea6446d981a627dcfe773624
Source noteuspto-grants-1999_03