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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49944Generated: October 27, 2026

Cyclopentanol → Ethyl 4-(t-butoxycarbonylamino)-2-cyclopentyloxybenzoate

https://huagongshe.com/reaction/49944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanolHCID 7298—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantEthyl 4-(t-Butoxycarbonylamino)-2-hydroxybenzoateHCID 17834349—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(t-butoxycarbonylamino)-2-cyclopentyloxybenzoateHCID 17834381—

Reaction Steps

A mixture of 460 mg of ethyl 4-(t-butoxycarbonylamino)-2-hydroxybenzoate, 300 mg of cyclopentanol, 1.5 g of diethyl azodicarboxylate (40% solution in toluene), 900 mg of triphenylphosphine and 10 ml of tetrahydrofuran was stirred at room temperature for 3 days. The solvent was evaporated and the residue was purified by the silica gel chromatography (ethyl acetate/hexane) to obtain crude ethyl 4-(t-butoxycarbonylamino)-2-cyclopentyloxybenzoate. A mixture of this crude product, 20 ml of ethanol and 5 ml of 1 M aqueous sodium hydroxide solution was stirred at room temperature overnight. After the treatment with ethyl acetate as the extracting solvent in an ordinary manner, the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710056B2
Source datasetuspto-grants-2004_03
ORD IDord-abec80d2a00946b3ba38919b8e07f98f
Source noteuspto-grants-2004_03