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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418859Generated: November 2, 2026

Oxalic Acid → N-(2-fluorophenyl)-1-pyrrolidinecarboximidamide

https://huagongshe.com/reaction/1418859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantPyrrolidineHCID 31268—
ReactantHCID 178503973HCID 178503973—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
ProductN-(2-fluorophenyl)-1-pyrrolidinecarboximidamideHCID 178511984—

Reaction Steps

To stirred solution of 2.0 g (0.006 mol) of N-(2-fluorophenyl)-S-methylisothiourea in 50 ml of ethanol was added 2.0 g (0.028 mol) of pyrrolidine and the reaction refluxed for eight hours. The solvent was then evaporated and to the residue was added 100 ml of water and 20 ml of 2N sodium hydroxide. The aqueous phase was then extracted with ethyl acetate (3×100 ml) and the organic phase dried over magnesium sulphate. Evaporation of the solvent gave a crude residue. This crude residue was then dissolved in 25 ml of hot isopropanol and oxalic acid was added in excess. Upon cooling a white solid crystallized and was collected by filtration and dried at 60° C. for 24 hours to give the oxalate salt of N-(2-fluorophenyl)-1-pyrrolidinecarboximidamide, M.P. 172°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885985
Source datasetuspto-grants-1999_03
ORD IDord-9f7b4d20dd1741f69fc08202b6c0172f
Source noteuspto-grants-1999_03