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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376973Generated: October 30, 2026

HCID 11726907, compound → 5-Acetoxy-4,6-di-tert-butyl-2,2-dimethyl-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/1376973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11726907HCID 11726907—
SolventN,N-DimethylanilineHCID 949—
Product5-Acetoxy-4,6-di-tert-butyl-2,2-dimethyl-2,3-dihydrobenzofuranHCID 10980083107.2%

Reaction Steps

4-Acetoxy-3,5-di-tert-butyl-1-(2-methyl-2-propenyloxy)benzene (2.22 g) was dissolved in N,N-dimethylaniline (8 ml) and the solution was refluxed under a nitrogen atmosphere for 36 h. After cooling to room temperature, the reaction solution was concentrated under reduced pressure and, after addition of 1N HCl (5 ml) and diethyl ether (10 ml), stirring was continued for 15 min. The organic layer was separated and the aqueous layer was subjected to extraction with diethyl ether. The combined extracts were washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (5% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butyl-2,2-dimethyl-2,3-dihydrobenzofuran [1.19 g (yield, 54%)] as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663373
Source datasetuspto-grants-1997_09
ORD IDord-e8a44f091f5d4ba087f4616b95e0647f
Source noteuspto-grants-1997_09