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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869253Generated: October 29, 2026

Trifluoroacetic acid → Benzyl (3-methoxy-4-piperidin-4-ylphenyl)carbamate

https://huagongshe.com/reaction/869253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(4-{[(benzyloxy)carbonyl]amino}-2-methoxyphenyl)piperidine-1-carboxylateHCID 66642793—
Solvent1,2-DichloroethaneHCID 11—
ProductBenzyl (3-methoxy-4-piperidin-4-ylphenyl)carbamateHCID 8666205485.2%

Reaction Steps

A mixture of tert-butyl 4-(4-{[(benzyloxy)carbonyl]amino}-2-methoxyphenyl)piperidine-1-carboxylate (Preparation Example 454) (4.92 g), trifluoroacetic acid (10 mL) and 1,2-dichloroethane (50 mL) was stirred at room temperature for 1 hour. The reaction solvent was concentrated under reduced pressure, and after addition of saturated aqueous sodium hydrogen carbonate, the residue was extracted with chloroform. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was solidified by addition of diethyl ether to give benzyl (3-methoxy-4-piperidin-4-ylphenyl)carbamate (3.24 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969336B2
Source datasetuspto-grants-2015_03
ORD IDord-2e0ed21dc2514555a4532f69df73fa75
Source noteuspto-grants-2015_03