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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900513Generated: October 25, 2026

5-Benzyloxy-4-t-butyl-2-formylbenzofuran → 4-t-Butyl-5-hydroxy-2-methylbenzofuran

https://huagongshe.com/reaction/1900513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-4-t-butyl-2-formylbenzofuranHCID 23442879—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product4-t-Butyl-5-hydroxy-2-methylbenzofuranHCID 2344286668.1%

Reaction Steps

5-Benzyloxy-4-tert-butyl-2-formylbenzofuran (700 mg, 2.3 mmol) was dissolved in acetic acid (30 ml) and, after addition of 10% Pd on carbon (700 mg), the solution was stirred under a hydrogen atmosphere (5 atm.) for 8 h. After filtering off the Pd on carbon, the filtrate was washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over anhydrous magnesium sulfate and concentrated. The concentrate was subjected to silica gel chromatography and eluted with a solvent system consisting of a 4:1 mixture of hexane and ethyl acetate to afford 4-tert-butyl-5-hydroxy-2-methylbenzofuran [320 mg (yield, 68%)] as a pale yellow, fine-grained crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574178
Source datasetuspto-grants-1996_11
ORD IDord-578969d7ffa1488d9ddb06d1ac217ac9
Source noteuspto-grants-1996_11