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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869252Generated: October 30, 2026

Tetrahydrofuran → Tert-butyl 4-(4-{[(benzyloxy)carbonyl]amino}-2-methoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/869252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-(4-amino-2-methoxyphenyl)piperidine-1-carboxylateHCID 66642900—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(4-{[(benzyloxy)carbonyl]amino}-2-methoxyphenyl)piperidine-1-carboxylateHCID 66642793—

Reaction Steps

To a mixture of tert-butyl 4-(4-amino-2-methoxy-phenyl)piperidine-1-carboxylate (Preparation Example 413) (4.25 g) and THF (100 mL), sodium hydrogen carbonate (1.28 g) and water (30 mL) were added, followed by dropwise addition of benzyl chloroformate (1.98 mL) under ice cooling and stirring overnight. After addition of water and extraction with ethyl acetate, the extract was washed with saturated aqueous sodium chloride. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=2:1) to give tert-butyl 4-(4-{[(benzyloxy)carbonyl]amino}-2-methoxyphenyl)piperidine-1-carboxylate (4.92 g) as a colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969336B2
Source datasetuspto-grants-2015_03
ORD IDord-1a466f8d8a674e789d2193fc5ee87527
Source noteuspto-grants-2015_03