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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566096Generated: October 31, 2026

Tetrahydrofuran → 7-(4-Fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylic acid

https://huagongshe.com/reaction/566096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18472577HCID 18472577—
SolventEthanolHCID 702—
Product7-(4-Fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylic acidHCID 1847228786%

Reaction Steps

To methyl 7-(4-fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate (0.27 g) were added THF (5.0 ml), ethanol (10.0 ml) and 2N sodium hydroxide solution (1.0 ml), and the mixture was stirred at room temperature for 19 hours. Under reduced pressure, the solvent was removed, and the residue was diluted with water (100 ml). The aqueous layer was made acidic with hydrochloric acid, and the mixture was extracted with ethyl acetate (100 ml). The organic layer was dried with anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was crystallized and washed with hexane to give 7-(4-fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylic acid (0.22 g, 86%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-06fa9c6e618843c6918d89ac531f5d7f
Source noteuspto-grants-2001_01