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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 178503973 | HCID 178503973 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-(2-fluorophenyl)-1-pyrrolidinecarboximidamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05885985 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-9f7b4d20dd1741f69fc08202b6c0172f |
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| Source note | uspto-grants-1999_03 |
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