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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443673Generated: October 29, 2026

HCID 53681655, compound → HCID 23468129, compound

https://huagongshe.com/reaction/443673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53681655HCID 53681655—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 23468129HCID 23468129—

Reaction Steps

3-{3-[3-[2-(1-Hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propenyl}benzoic acid (7.8 g., 0.02 mole) (the compound of Example 11) in ethanol (125 ml.) is hydrogenated over 2.5 g. of a 5% Pd on charcoal catalyst at 1 atmosphere pressure and 27° C. When the theoretical amount (0.02 mole) of hydrogen has been absorbed, the catalyst is filtered off, the solvent evaporated, and the residue chromatographed on silica gel with 4% methanol in chloroform as the eluant. The title compound is obtained as a colorless, viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260771
Source datasetuspto-grants-1981_04
ORD IDord-9954d6c52b11456eacdae95134ef5026
Source noteuspto-grants-1981_04