Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900529Generated: October 29, 2026

HCID 22918668, compound → HCID 22918658, compound

https://huagongshe.com/reaction/1900529

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 numberUS05574178
Source datasetuspto-grants-1996_11
ORD IDord-024d21d5a0364ffa85b90b45f2bf614f
Source noteuspto-grants-1996_11