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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797263Generated: October 30, 2026

Trifluoroacetic acid → (R)-3-amino-4-[4-(4-fluorophenoxy)-piperidin-1-yl]-butyric acid benzyl ester

https://huagongshe.com/reaction/1797263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(R)-3-tert-butoxycarbonylamino-4-[4-(4-fluoro-phenoxy)-piperidin-1-yl]butyric acid benzyl esterHCID 68576098—
SolventDichloromethaneHCID 6344—
Product(R)-3-amino-4-[4-(4-fluorophenoxy)-piperidin-1-yl]-butyric acid benzyl esterHCID 68576481—

Reaction Steps

A solution of (R)-3-tert-butoxycarbonylamino-4-[4-(4-fluoro-phenoxy)-piperidin-1-yl]-butyric acid benzyl ester (0.488 g, 1.0 mmol) in DCM (8 ml) is treated with trifluoroacetic acid (2 ml). The reaction mixture is stirred at ambient temperature for 1 hour. The solvent is evaporated and the residue taken up in DCM and washed with saturated aqueous NaHCO3. The organic phase is dried over MgSO4 and evaporated to yield (R)-3-amino-4-[4-(4-fluorophenoxy)-piperidin-1-yl]-butyric acid benzyl ester. [MH]+ 387.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034042B2
Source datasetuspto-grants-2006_04
ORD IDord-5c4e12ecc1c7492084993ba09c04b88f
Source noteuspto-grants-2006_04