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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452386Generated: October 31, 2026

HCID 22918668, compound → HCID 22918658, compound

https://huagongshe.com/reaction/1452386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22918668HCID 22918668—
SolventAcetic AcidHCID 176—
ProductHCID 22918658HCID 22918658—

Reaction Steps

5-Acetoxy-2-[2-(1,3-dioxa-2-cyclopentyl)ethyl]-4,6-di-tert-butyl-2-methyl-2,3-dihydrobenzofuran (17.3 g) was dissolved in 80% acetic acid (150 ml) and the solution was heated under reflux for 1 h. After cooling the solution, the acetic acid was distilled off under vacuum and, after addition of water, the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (25% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butyl-2-(2-formylethyl)-2-methyl-2,3-dihydrobenzofuran quantitatively (15.53 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606089
Source datasetuspto-grants-1997_02
ORD IDord-5680c654e8154e319b0ec333af18ded0
Source noteuspto-grants-1997_02