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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376998Generated: November 1, 2026

5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuran → 5-Acetoxy-4,6-di-tert-butyl-2-octylbenzofuran

https://huagongshe.com/reaction/1376998

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuranHCID 53768721—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-Acetoxy-4,6-di-tert-butyl-2-octylbenzofuranHCID 1843317696%

Reaction Steps

5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuran (3.1 g) was dissolved in ethyl acetate containing 10% acetic acid (50 ml) and, after addition of 10% Pd on carbon (0.3 g), the solution was stirred under a hydrogen atmosphere for 3 h. After filtering off the Pd on carbon, the filtrate was concentrated under vacuum. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butyl-2-Octylbenzofuran [2.95 g (yield, 96%)] as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663373
Source datasetuspto-grants-1997_09
ORD IDord-b485bb6deea448ffa3c881a4adac21a3
Source noteuspto-grants-1997_09