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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900495Generated: October 26, 2026

5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran → 4-Tert-butyl-5-hydroxy-2-octylbenzofuran

https://huagongshe.com/reaction/1900495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuranHCID 54308722—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product4-Tert-butyl-5-hydroxy-2-octylbenzofuranHCID 2344286469%

Reaction Steps

10% Palladium on carbon (1.1 g) was added to a solution of 5-benzoxy-4-tert-butyl-2-(1-octenyl)benzofuran (1.1 g, 2.9 mmol) in acetic acid (50 ml), and the mixture was stirred for 36 h under a hydrogen atmosphere. After filtering off the Pd on carbon, the solvent was distilled off with an evaporator. The concentrate was purified by silica gel chromatography (chloroform) to afford 4-tert-butyl-5-hydroxy-2-octylbenzofuran [600 mg (yield, 69%)] as a pale yellow oil. Mass 302(M+), 287, 57

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574178
Source datasetuspto-grants-1996_11
ORD IDord-654044c7f52a410ca77eb26a111baa4e
Source noteuspto-grants-1996_11