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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615398Generated: November 2, 2026

HCID 86674531, compound → HCID 71073896, compound

https://huagongshe.com/reaction/1615398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86674531HCID 86674531—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 71073896HCID 71073896—

Reaction Steps

The 4-(4-tert-butoxycarbonylaminopiperidin-1-yl)-cinnamic acid ethyl ester (126 g, 0.33 mol) obtained in Example 8 (1) was dissolved in ethanol (1 L), and 10% Pd—C (48.5 g) was added, followed by stirring in a hydrogen atmosphere for 18 hours. The insoluble material was filtered with Celite, and the filtrate was evaporated under reduced pressure, thereby obtaining 4-(4-tert-butoxycarbonylaminopiperidin-1-yl)-dihydrocinnamic acid ethyl ester (107 g, 85%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765750B2
Source datasetuspto-grants-2014_07
ORD IDord-133e994024a8477096d89ab01d877eb4
Source noteuspto-grants-2014_07