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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225552Generated: October 30, 2026

HCID 178418361, compound → HCID 178490122, compound

https://huagongshe.com/reaction/2225552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178490123HCID 178490123—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 178490122HCID 17849012280.7%

Reaction Steps

3.62 g of N-(trans-4-methylcyclohexyl)-4-(4-benzyloxy-3-methoxyphenyl)-l,3-butadiene-1-carboxamide (Example 117) was dissolved in 150 ml of methanol. 0.2 g of 10% palladium-carbon was added to the solution. The solution was stirred for 16 hours under normal-pressure hydrogen gas. After reaction, the catalyst was filtered out, and the solvent was removed in vacuo from the filtrate, yielding 2.3 g of N-(trans-4-methylcyclohexyl)-5-(4-hydroxy-3-methoxyphenyl)valeramide (a compound of the present invention) as a pale yellow oil, which had the following physiochemical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344845
Source datasetuspto-grants-1994_09
ORD IDord-e10504eca05e454e900f09859108711d
Source noteuspto-grants-1994_09