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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333448Generated: October 29, 2026

Trifluoroacetic acid → 1-(4-Cyclohexylpiperidin-4-yl)butan-1-one

https://huagongshe.com/reaction/333448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-butyryl-4-cyclohexylpiperidine-1-carboxylateHCID 66987675—
SolventDichloromethaneHCID 6344—
Product1-(4-Cyclohexylpiperidin-4-yl)butan-1-oneHCID 66987849119.5%

Reaction Steps

2.5 g (7.4 mmol) of tert-butyl 4-butyryl-4-cyclohexylpiperidine-1-carboxylate (cf. preparation 17-1-4) are diluted in a mixture comprising 40 mL of dichloromethane and 8 mL of trifluoroacetic acid. The mixture is stirred at room temperature for 2 hours and the reaction is then stopped by adding aqueous 1N NaOH solution and the organic compounds are extracted with dichloromethane. The organic phase is dried and then concentrated. 2.1 g of 1-(4-cyclohexylpiperidin-4-yl)butan-1-one in the form of a colourless oil are obtained in a yield of 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877968B2
Source datasetuspto-grants-2014_11
ORD IDord-f99ab9da94334c9b82460196afd9b3f5
Source noteuspto-grants-2014_11