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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78027Generated: October 26, 2026

4-((E)-2-furan-2-yl-vinyl)benzoic acid ethyl ester → 4-(2-Furan-2-yl-ethyl)-benzoic acid ethyl ester

https://huagongshe.com/reaction/78027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((E)-2-furan-2-yl-vinyl)benzoic acid ethyl esterHCID 59255067—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Furan-2-yl-ethyl)-benzoic acid ethyl esterHCID 5925511065.7%

Reaction Steps

To an anhydrous tetrahydrofuran (25 mL) solution of 4-((E)-2-furan-2-yl-vinyl)-benzoic acid ethyl ester (1.07 g, 4.4 mmol) described in Manufacturing Example 80-1-1 was added 10% palladium-carbon (50% hydrate, 500 mg), which was added for 2 hours under a hydrogen atmosphere at room temperature. The reaction product was filtered, and the filtrate was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (t-butylmethyl ether: heptane=5:95) to obtain the title compound (706 mg, 65.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-879415cde28647bcbb44f517524588a4
Source noteuspto-grants-2014_09