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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499187Generated: October 30, 2026

Trifluoroacetic acid → HCID 23103401, compound

https://huagongshe.com/reaction/499187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant{4-[1-(2,6-Dichloro-benzoyl)-piperidin-4-yloxy]-phenyl}-carbamic acid tert-butyl esterHCID 59420870—
SolventDichloromethaneHCID 6344—
ProductHCID 23103401HCID 2310340192%

Reaction Conditions

Temperature22 °C

Reaction Steps

The above white solid, {4-[1-(2,6-dichloro-benzoyl)-piperidin-4-yloxy]-phenyl}-carbamic acid tert-butyl ester, is suspended in a solution of trifluoroacetic acid in dichloromethane (25% v/v, 20 mL). The reaction mixture is stirred at 22° C. for 15 min. After removal of the solvent, the oily residue is neutralized with 0.5 N aqueous sodium hydroxide solution (50 mL) and extracted with dichloromethane (5×50 mL). The combined organic phases are dried over anhydrous sodium sulfate and concentrated to yield a yellow solid (440.2 mg, 92.0% yield, ES+(m/z) 365.1 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767674B2
Source datasetuspto-grants-2010_08
ORD IDord-a8eb332209a84b3aa709d5b81503900b
Source noteuspto-grants-2010_08