Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900506Generated: October 30, 2026

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

https://huagongshe.com/reaction/1900506

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. Mass 304(M+), 289, 163, 57

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574178
Source datasetuspto-grants-1996_11
ORD IDord-4b21c77105324461ab3f27a8b47b9122
Source noteuspto-grants-1996_11