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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289432Generated: October 25, 2026

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

https://huagongshe.com/reaction/2289432

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 numberUS06093710
Source datasetuspto-grants-2000_07
ORD IDord-b734d03058194cb3b02b48b65a261790
Source noteuspto-grants-2000_07