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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452363Generated: October 31, 2026

Water → 4,6-Di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/1452363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant5-Acetoxy-4,6-di-tert-butyl-2,2-diethyl-2,3-dihydrobenzofuranHCID 11024452—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4,6-Di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuranHCID 1109875787%

Reaction Steps

Lithium aluminum hydride (76 mg) was suspended in tetrahydrofuran (5 ml) under a nitrogen atmosphere. A solution of 5-acetoxy-4,6-di-tert-butyl-2,2-diethyl-2,3-dihydrobenzofuran (0.17 g, 0.5 mmol) in tetrahydrofuran (5 ml) was added dropwise to the suspension. After heating under reflux for 3 h, the reaction mixture was cooled to room temperature and water was added dropwise. After addition of 1N aqueous sodium hydroxide (5 ml), the mixture was subjected to extraction with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 4,6-di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuran [130 mg (yield, 87%)] as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606089
Source datasetuspto-grants-1997_02
ORD IDord-9a59f57a4fca448b8eb8786fa519473a
Source noteuspto-grants-1997_02