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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium ChlorideHCID 5234—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantTert-butyl 2-(aminocarbonyl)-4-fluoropyrrolidine-1-carboxylateHCID 17856474—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl (2S,4S)-2-cyano-4-fluoropyrrolidine-1-carboxylateHCID 18453438—

Reaction Conditions

Temperature2.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893103B2
Source datasetuspto-grants-2011_02
ORD IDord-0e09863d8d584b99a237c15fc84ea1f2
Source noteuspto-grants-2011_02