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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433746Generated: October 26, 2026

Pyridine → (1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1433746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
Reactant(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acidHCID 7021178—
SolventDichloromethaneHCID 6344—
Product(1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl esterHCID 87517560—

Reaction Steps

To a solution of (2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid (838 mg, 3.0 mmol) in dichloromethane (10 mL) at −35° C. was added dry pyridine (255 μL, 3.15 mmol) and cyanuric fluoride (375 μL, 4.5 mmol) under an atmosphere of dry argon. The mixture was stirred for 1.5 hours while maintaining the temperature between −35 and −25° C. A small amount of ice was added to the reaction mixture and the mixture stirred vigorously for 15 minutes. The organic layer was decanted away from the aqueous solution and the aqueous layer extracted with dichloromethane (2×10 mL). The combined organic layers were washed with ice cold water (15 mL), dried over sodium sulfate, filtered and concentrated in vacuo to give (1-fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester which was used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612212B2
Source datasetuspto-grants-2009_11
ORD IDord-0dfd7448cbba4e059c35e0105354547d
Source noteuspto-grants-2009_11