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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74902Generated: October 26, 2026

Trifluoroacetic anhydride → Tert-butyl 2-cyano-4,4-difluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/74902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantTert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylateHCID 67286514—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductTert-butyl 2-cyano-4,4-difluoropiperidine-1-carboxylateHCID 67284864—

Reaction Steps

To a solution of tert-butyl 2-carbamoyl-4,4-difluoro-piperidine-1-carboxylate, 13g, (1.72 g, 6.51 mmol) in CH2Cl2 (50 mL) was added was N,N-triethylamine (2.03 mL, 14.61 mmol) followed by the dropwise addition of (2,2,2-trifluoroacetyl)-2,2,2-trifluoroacetate (1.02 mL, 7.32 mmol). After 15 minutes, the mixture was diluted with aqueous saturated NaHCO3 solution and the layers were separated. The organic phase was washed with water, dried over Na2SO4, filtered and evaporated to dryness. The crude residue was passed through a plug of silica gel and eluted with 10-30% EtOAc/hexanes to afford the desired product, 13h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829007B2
Source datasetuspto-grants-2014_09
ORD IDord-c409c9554e0042f3a22511bb23544bf9
Source noteuspto-grants-2014_09