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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222575Generated: October 28, 2026

Trifluoroacetic acid → HCID 66865450, compound

https://huagongshe.com/reaction/222575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
Reactant1-Piperidinecarboxylic acid, 4-[[4-[1,2,3,6-tetrahydro-1-(methylsulfonyl)-4-pyridinyl]phenoxy]methyl]-, 1,1-dimethylethyl esterHCID 66864688—
SolventDichloromethaneHCID 6344—
ProductHCID 66865450HCID 6686545088.5%

Reaction Conditions

Temperature23 °C

Reaction Steps

Trifluoroacetic acid (2.98 g, 1.97 mL, 26.10 mmol) is added to a solution of 4-[4-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester (1.20 g, 2.61 mmol) in dichloromethane (13 mL). The mixture is stirred at 23° C. for 30 min. 2 M aq. sodium hydroxide is added. The resulting white precipitate is filtered and washed with water. The mother liquor is extracted with dichloromethane. The combined organic layers are dried over anhydrous sodium sulfate, filtered, and the solvent is removed to obtain a white solid which is combined with the initial precipitate and dried under high vacuum for 16 h. Diethyl ether is added and the solid is filtered and washed with ethyl acetate to obtain 0.810 g of an off-white solid. MS (m/z) 351 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207344B2
Source datasetuspto-grants-2012_06
ORD IDord-5c024ea63cd54bffab2429acb24fa1ae
Source noteuspto-grants-2012_06