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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186267Generated: October 30, 2026

HCID 23442874, compound → HCID 53674989, compound

https://huagongshe.com/reaction/2186267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23442874HCID 23442874—
SolventN,N-DimethylanilineHCID 949—
ProductHCID 53674989HCID 53674989179.2%

Reaction Steps

Under a nitrogen stream, a solution of 0.48 g of 2,5-di-t-butyl-4-trimethylacetoxy-1-(2-methyl-2-propenyloxy)benzene in 5 ml of dimethylaniline was refluxed overnight. The solution was allowed to attain room temperature and concentrated under reduced pressure, then extracted with ethyl acetate and 5% hydrochloric acid. The organic layers were washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated. The concentrate was purified by silica gel column chromatography (in n-hexane containing 0.5% ethyl acetate) to give 0.43 g of 4,7-di-t-butyl-2,2-dimethyl-5-trimethylacetoxy-2,3-dihydrobenzofuran as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403639B1
Source datasetuspto-grants-2002_06
ORD IDord-48f7cdf4de0247d59605021c05aa3532
Source noteuspto-grants-2002_06