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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254890Generated: October 25, 2026

Cyclohexene → 7-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran

https://huagongshe.com/reaction/254890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
Reactant7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyranHCID 59592104—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product7-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyranHCID 985984794.9%

Reaction Steps

Cyclohexene (1.5 mL) and Pd(OH)2/C (0.15 g) were added to a solution of compound 1 (0.3 g, 0.87 mmol) in ethanol (20 mL). The resultant mixture was stirred under a reflux temperature of 78° C. for 2 hrs, and then cooled to room temperature. After filtration, the filtrate was concentrated in vacuo, followed by purification via silica gel column chromatography (ethyl acetate/n-hexane=1:4), thus giving the title compound 3a as a colorless crystal (0.21 g, 94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875735B2
Source datasetuspto-grants-2011_01
ORD IDord-e419364d7b0c47459d06fad7341fe4f6
Source noteuspto-grants-2011_01