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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166953Generated: October 31, 2026

Methane → HCID 13174427, compound

https://huagongshe.com/reaction/2166953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHCID 13174425HCID 13174425—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
ProductHCID 13174427HCID 13174427—

Reaction Steps

Step 2, Hydrogenation Process (Ethyl Ester): 99.1 g of crude alpha-hydroxy-(4-methyl-2-oxo-3-cyclopenten-1-yl)-acetic acid ethyl ester (as prepared in Example 1) in 882 ml of toluene was hydrogenated over 9.91 g of 10% by weight of palladium and 90% by weight of charcoal at room temperature and 25-50 psi. After hydrogen uptake had ceased, the catalyst and solvent were removed by filtration and evaporation to give 101 g of a viscous, amber-colored oil. This oil is distilled to provide the product alpha-hydroxy-4-methyl-2-oxo-cyclopentane acetic acid ethyl ester, bp 96°-111°/0.05 mmHg, for use in Example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04390718
Source datasetuspto-grants-1983_06
ORD IDord-403e75845c6f43aea55cfba886ffb68e
Source noteuspto-grants-1983_06