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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862725Generated: November 2, 2026

Tetrahydrofuran → HCID 586422, compound

https://huagongshe.com/reaction/1862725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-ThiophenecarboxaldehydeHCID 68135—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 586422HCID 586422—

Reaction Steps

A suspension of potassium t-butoxide (61.5 g, 0.55 mol) in THF (800 mL) was cooled in an ice bath and trimethylphospbonoacetate (98 mL, 0.60 mol) in THF (100 mL) was slowly added. After 45 min, thiophene 3-carboxaldehyde (50 mL, 0.55 mol) in THF (100 mL) was slowly added while stirred in the ice bath. The mi,suture was allowed to warm to rt and stirred for 16 h. The reaction was quenched with 5% sulfuric acid (300 mL) and extracted twice with ether. The organic layers were each washed with brine, dried over magnesium sulfate, combined and concentrated. The residue was purified by FC (10% ethyl acetate in hexanes) and then crystallized from hexanes to give the title compound (71.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538002B1
Source datasetuspto-grants-2003_03
ORD IDord-0de1b2d591174c5b97185d9416623462
Source noteuspto-grants-2003_03