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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518815Generated: November 1, 2026

Trifluoroacetic acid → Piperidin-4-yl acetate

https://huagongshe.com/reaction/518815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-acetoxypiperidine-1-carboxylateHCID 21660336—
SolventDichloromethaneHCID 6344—
ProductPiperidin-4-yl acetateHCID 112520759.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

3 ml of trifluoroacetic acid are added to a solution of 3.18 g of 2-methylpropan-2-yl 4-(acetyloxy)piperidine-1-carboxylate in 40 ml of dichloromethane, cooled to 0° C. The reaction medium is stirred for 1 hour at 0° C. and then 1 hour at ambient temperature. 5 ml of trifluoroacetic acid are added and the reaction medium is stirred for 30 minutes at ambient temperature. The reaction medium is evaporated to dryness under reduced pressure, and the resulting product is taken up with dichloromethane and an aqueous 1% NH4OH solution. The organic phase is washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and evaporated, so as to give 175 mg of piperidin-4-yl acetate in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-4b146fa514ef4288974d0a23e806d69d
Source noteuspto-grants-2015_08