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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615393Generated: November 2, 2026

Water → Ethyl 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)benzoate

https://huagongshe.com/reaction/1615393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl 4-(4-aminopiperidin-1-yl)benzoateHCID 22557718—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)benzoateHCID 66691942—

Reaction Steps

The 4-(4-aminopiperidin-1-yl)-benzoic acid ethyl ester (15.7 g, 63.2 mmol) obtained in Example 7(1) was dissolved in THF (200 ml), and a 2M sodium carbonate aqueous solution (63 ml) was added thereto. Subsequently, benzyloxycarbonyl chloride (11.7 ml, 82.2 mmol) was added thereto, followed by stirring at room temperature for 2 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated sodium chloride, and then dried over anhydrous sodium sulfate. After the desiccant was filtered off, the solid obtained by evaporation under reduced pressure was collected by filtration and dried under reduced pressure, thereby obtaining 4-(4-benzyloxycarbonylaminopiperidin-1-yl)-benzoic acid ethyl ester (18.0 g, 74%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765750B2
Source datasetuspto-grants-2014_07
ORD IDord-feb08f97bd674ff7bcfd344a649b6494
Source noteuspto-grants-2014_07