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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650595Generated: October 27, 2026

Tetrahydrofuran → 4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furan

https://huagongshe.com/reaction/650595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant4,5,6,7-Tetrahydro-1-benzofuran-4-oneHCID 2733541—
ReactantHCID 178418682HCID 178418682—
SolventEthyl AcetateHCID 8857—
Product4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furanHCID 54518756—

Reaction Steps

To a mixture of 4-oxo-4,5,6,7-tetrahydrobenzo[b]furan (20.06 g) and THF (200 ml) was added dropwise 2M n-butylmagnesium bromide with ice-water cooling over 15 minutes. The mixture was stirred at r.t. overnight. The reaction mixture was poured into a mixture of a saturated aqueous solution of NH4Cl and AcOEt. The separated organic layer was washed with water and brine, and dried over MgSO4, and evaporated. The resulting oil was purified by chromatography on SiO2 (CHCl3 as eluent) to give 4-n-butylidene-4,5,6,7-tetrahydrobenzo[b]furan as a yellow oil (12.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274619B1
Source datasetuspto-grants-2001_08
ORD IDord-274df34808e2475186d75710ee35a1fe
Source noteuspto-grants-2001_08