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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878364Generated: November 1, 2026

Trifluoroacetic acid → HCID 86670823, compound

https://huagongshe.com/reaction/878364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86670824HCID 86670824—
SolventDichloromethaneHCID 6344—
ProductHCID 86670823HCID 86670823—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of cyanomethyl-[4-(2-trifluoromethoxy-phenyl)-pyridin-3-yl]-carbamic acid tert-butyl ester (185 mg, 0.47 mmol) in CH2Cl2 (5 mL) was added trifluoroacetic acid (1 mL) at 0° C. The reaction mixture was stirred at 25° C. for 2 hours and then concentrated under vacuum. The residue was dissolved in 10 mL aqueous sodium bicarbonate solution and 20 mL CH2Cl2 and the layers were separated. The aqueous layer was extracted again with 10 mL CH2Cl2. The combined organic layer was washed with 20 mL brine, dried over Na2SO4, filtered and concentrated under vacuum. The resulting light yellow solid was pure enough to be used in the next step without further purification (115 mg, 83%). LC-MS (ESI): m/z=294.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987307B2
Source datasetuspto-grants-2015_03
ORD IDord-05d6c2d83d2b42859c9604124a553a0e
Source noteuspto-grants-2015_03