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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464418Generated: October 30, 2026

Phosgene → HCID 13534257, compound

https://huagongshe.com/reaction/464418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantHCID 20263002HCID 20263002—
SolventBenzeneHCID 241—
ProductHCID 13534257HCID 135342574.4%

Reaction Steps

To a stirred solution of 275 ml of 2 molar phosgene (0.55 mole) in benzene under nitrogen gas was added dropwise a solution of 0.5 mole of 1-benzyl-3-(3,4-dichlorophenoxy)pyrrolidine in 200 ml of dry benzene. The reaction mixture was stirred an additional 0.5 hr, then was filtered to remove 10 g of the starting pyrrolidine compound as the hydrochloric acid salt. The filtrate was concentrated under reduced pressure to give an oil. The oil was triturated four times in succession with 200 ml each of 30/60 petroleum ether which removed most of the benzyl chloride by-product. The combined petroleum ether when cooled gave 6.5 g of white crystal product which was separated by filtration. The oil residue, after removing excess petroleum ether under vacuum, crystallized. The crystals were separated by filtration and washed with petroleum ether to give 93 g of tan-colored material. Further work-up of the last petroleum ether filtrate gave 17 g additional crude product. Combined yield of crude tan product was 116.5 g (70%), m.p. 79°-84° C. A portion of the crude was recrystallized from 30/60 petroleum ether to give white crystalline product, m.p. 79°-84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547514
Source datasetuspto-grants-1985_10
ORD IDord-13201512520347bd9e479eef87c3161e
Source noteuspto-grants-1985_10