Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430769Generated: October 30, 2026

Tetrahydrofuran → HCID 18351660, compound

https://huagongshe.com/reaction/430769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant7-methoxy-1-benzofuran-3-carboxylic acidHCID 12844603—
Reactant1-Hydroxy-4-phenylbutan-2-oneHCID 15090463—
ProductHCID 18351660HCID 1835166047%

Reaction Steps

7-methoxybenzofuran-3-carboxylic acid (220 mg) was dissolved in THF (5 ml). To this solution, 4-phenyl-2-oxo-1-butanol (211 mg) and dicyclohexylcarbodiimide (330 mg) were added and the resulting solution was stirred at room temperature for 16 hours. The reaction solution was filtered and the filtrate was poured into water layer (50 ml), followed by extraction twice with ethyl acetate (20 ml). The organic layers were combined and washed with saturated brine, followed by drying over sodium sulfate. After removing the sodium sulfate by filtration, the solvent was removed under reduced pressure and the residue was purified by column chromatography (solvent: hexane/ethyl acetate=3/1) using silica gel to obtain the desired compound (178 mg, yield: 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323235B1
Source datasetuspto-grants-2001_11
ORD IDord-3899f041d5c7434fa90e5f89861b1b1a
Source noteuspto-grants-2001_11