HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367115Generated: October 29, 2026
Imidazole → tert-Butyl (2S,4S)-2-cyano-4-fluoropyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1367115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Tert-butyl 2-(aminocarbonyl)-4-fluoropyrrolidine-1-carboxylate | HCID 17856474 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl (2S,4S)-2-cyano-4-fluoropyrrolidine-1-carboxylate | HCID 18453438 | — |
Reaction Steps
In a 5.0 L 4-necked RB flask, fitted with a mechanical stirrer and reflux condenser, pyridine (1000 ml) and imidazole (58.6 gm, 0.86 mol) were added at 25-35° C. while stirring. The reaction mixture was cooled to 0-5° C. while stirring for 30 min, tert-butyl 2-(aminocarbonyl)-4-fluoropyrrolidine-1-carboxylate (100 gm, 0.43 mol) and phosphorous oxychloride (165.7 gm, 1.07 mol) were added slowly at 0-5° C. while stirring. After addition, the reaction mixture was maintained for 1 hr. The progress of the reaction was monitored by TLC. After ascertaining completion of the reaction by TLC, the reaction mixture was poured into an ice cold water (5 L), sodium chloride and ethylacetate (800 ml) mixture. The aqueous layer was washed with an ethyl acetate (800 ml), dilute HCl (4 100), sodium bicarbonate and saturated brine solution. The ethylacetate layer was distilled below 55° C. under vacuum and hexane (500 ml) was added to the resulting mass. Trace ethylacetate was distilled off. The resulting mass was taken as such to the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893103B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-0e09863d8d584b99a237c15fc84ea1f2 |
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| Source note | uspto-grants-2011_02 |
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