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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464429Generated: October 30, 2026

Water → HCID 13534234, compound

https://huagongshe.com/reaction/464429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant3-(2,3-Dichlorophenoxy)-1-pyrrolidinecarbonyl ChlorideHCID 20263011—
SolventChloroformHCID 6212—
ProductHCID 13534234HCID 13534234—

Reaction Steps

A solution 11.8 g (0.04 mole) of 3-(2,3-dichlorophenoxy)-1-pyrrolidinecarbonyl chloride in 50 ml of chloroform was stirred at 5° C. in an ice bath while the following were added in order: 25 g of ice, 5.52 g of potassium carbonate and 3.87 g (0.044 mole) of N,N-dimethylethylenediamine. The resulting mixture was stirred for 20 hours and worked up by adding additional water followed by separation of the organic phase. The chloroform solution was dried over magnesium sulfate, filtered and concentrated in vacuo to a dark amber oil, 14 g, which solidified on standing. TLC analysis (10% methanol/chloroform) showed 3 spots; therefore, the crude product was chromatographed on 50 g of Fluorisil. Elution with chloroform gave a dark forerun which was discarded, the main portion was collected and rechromatographed through a 50 g Florisil column. The column was washed with 200 ml of methanol and the 2 fractions (chloroform and methanol) were combined before concentrating on a rotary evaporator to give a light amber oil which solidified. Recrystallization from isopropyl ether gave a beige crystalline product; 4.5 g (34%), m.p. 94°-95° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547514
Source datasetuspto-grants-1985_10
ORD IDord-e66b923a75a043cfad254d5990fda233
Source noteuspto-grants-1985_10