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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422670Generated: November 3, 2026

Ethylparaben → tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/2422670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylparabenHCID 8434—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylateHCID 1178305062.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 4-hydroxybenzoate (4.15 g, 25.0 mmol), tert-butyl 4-hydroxytetrahydro-1(2H)-pyridinecarboxylate (5.0 g, 25.0 mmol) and triphenyl phosphine (7.87 g, 30.0 mmol) were dissolved in tetrahydrofuran (50 mL), and with stirring at 0° C., diisopropyl azodicarboxylate (6.06 g, 30.0 mmol) was added thereto and stirred for 24 hours. The reaction solution was concentrated, and the precipitated white solid was taken out through filtration and washed with ethyl acetate. The mother liquid was washed with aqueous 1 N sodium hydroxide solution and saturated saline water in that order, and the organic layer was dried with magnesium sulfate. The solvent was evaporated off, and the residue was purified through silica gel column chromatography (hexane/ethyl acetate=9/1) to obtain the intended compound (5.45 g, 62%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960394B2
Source datasetuspto-grants-2011_06
ORD IDord-35ab6affdc9345f5b626684df2fe7ca4
Source noteuspto-grants-2011_06