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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643531Generated: October 30, 2026

Furfural → Benzofuran

https://huagongshe.com/reaction/1643531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium CarbonateHCID 11430—
ReactantDiethyl SuccinateHCID 31249—
ReactantSodium AcetateHCID 517045—
ReactantDihydrobezofuranHCID 5857314—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
Solventtert-ButanolHCID 6386—
ProductBenzofuranHCID 9223—

Reaction Steps

As depicted in Scheme F, dihydrobenzofuran intermediate F-3 could be prepared starting from commercially available 2-furaldehyde and diethyl succinate. Treatment of 2-furaldehyde and diethyl succinate with potassium t-butoxide in refluxing t-butanol gives intermediate F-1. Treatment of F-1 with sodium acetate in refluxing acetic anhydride, followed by aqueous work-up and subsequently refluxing the residue in EtOH in the presence of K2CO3, gives benzofuran F-2. F-2 could be subjected to hydrogenation conditions to provide dihydrobenzofuran F-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-85cdb687fa3d4a11a8a9f11dec122a49
Source noteuspto-grants-2012_02