Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597286Generated: October 30, 2026

HCID 70609976, compound → HCID 70637287, compound

https://huagongshe.com/reaction/597286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70609976HCID 70609976—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 70637287HCID 70637287—

Reaction Steps

3-Phenyl-7-benzofuranacetic acid (2.5 g., 0.01 mole) is reduced with hydrogen gas using palladium on charcoal as catalyst and ethanol as solvent in a Brown hydrogenator. After the absorption of hydrogen stops, the reaction mixture is filtered, then the filtrate is evaporated in vacuo to a white solid. Recrystallization from a benzene-hexane mixture gives white crystals of 2,3-dihydro-3-phenyl-7-benzofuranacetic acid, m.p. 110.5°-111.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04013692
Source datasetuspto-grants-1977_03
ORD IDord-b1eced47cc594007977107f03ae61a7f
Source noteuspto-grants-1977_03