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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193054Generated: November 4, 2026

Methanol → Tert-butyl(3-phenylpropyl)(piperidin-4-yl)carbamate

https://huagongshe.com/reaction/2193054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl(3-phenylpropyl)(1-(trifluoroacetyl)piperidin-4-yl)carbamateHCID 59397931—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl(3-phenylpropyl)(piperidin-4-yl)carbamateHCID 59398435—

Reaction Steps

To 2 mL of a methanol solution containing 0.60 g of tert-butyl(3-phenylpropyl)(1-(trifluoroacetyl)piperidin-4-yl)carbamate, 0.4 mL of water was added, and 0.28 g of potassium carbonate was added under cooling with ice, and the mixture was stirred at the same temperature for 2 hours and 10 minutes and at room temperature for 2 hours and 15 minutes. Thereto was added 2 mL of methanol and 0.5 mL of water, and the mixture was left to stand at room temperature overnight. The solvent was removed under reduced pressure, and the residue thus obtained was added with ethyl acetate and water. The organic layer was separated, washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.45 g of a colorless oily substance, tert-butyl(3-phenylpropyl)(piperidin-4-yl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-e01bcad14e7545dca06dca1c4d12037a
Source noteuspto-grants-2012_12