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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434352Generated: October 25, 2026

2,5-Dichlorobenzenesulfonyl chloride → 2,4-Dimethyl-1-[3-(2,5-dichlorbenzenesulphonamido)propyl]-pyrrolidine

https://huagongshe.com/reaction/434352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichlorobenzenesulfonyl chlorideHCID 79401—
Reactant2,4-Dimethyl-1-(3-aminopropyl)pyrrolidineHCID 20227735—
SolventBenzeneHCID 241—
Product2,4-Dimethyl-1-[3-(2,5-dichlorbenzenesulphonamido)propyl]-pyrrolidineHCID 2022777267%

Reaction Steps

2,4-Dimethyl-1-(3-aminopropyl) pyrrolidine in (4.7 g, 0.03 mol) benzene (30 ml) was added dropwise at room temperature to a solution of 2,5-dichlorobenzenesulphonylchloride (7.3 g, 0.03 ml) in benzene (100 ml). Thereafter, the mixture was stirred for 4 days at room temperature until the reaction was complete. Finally, the reaction product was obtained as a viscous, oily paste. The benzene mother liquor was decanted. The residue was dissolved in water, the solution was adjusted to pH 9.8 with 10% NaOH and extractes with petroleum ether (40°-60°) (4×100 ml). The combined extracts were dried over Na2SO4 and evaporated. The residue (5 g) was recrystallised twice from 100 ml petroleum ether to yield the product (3.7 g as white needles), m.p. 65°-67° C. Yield=67% of theoretical

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04396622
Source datasetuspto-grants-1983_08
ORD IDord-9502282353894b94bbbb8e8dada3f36c
Source noteuspto-grants-1983_08