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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | (2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acid | HCID 7021178 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612212B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-0dfd7448cbba4e059c35e0105354547d |
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| Source note | uspto-grants-2009_11 |
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