Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530978Generated: October 31, 2026

Tetrahydrofuran → 2-Cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carbaldehyde

https://huagongshe.com/reaction/530978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 2-cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carboxylateHCID 90423848—
SolventWaterHCID 962—
Product2-Cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carbaldehydeHCID 9042358885.7%

Reaction Steps

A THF (50 mL) solution of ethyl 2-cyclopropyl-6-ethoxy-4′-fluorobiphenyl-4-carboxylate (10.5 g) was added to a THF (50 mL) suspension of lithium aluminum hydride (1.21 g) under ice cooling in a nitrogen atmosphere. After stirring at the same temperature as above for 30 minutes, water (1.2 mL) and a 15% aqueous sodium hydroxide solution (1.2 mL) were added thereto, and the mixture was stirred for 5 minutes. Water (3.6 mL) was further added to the reaction mixture, and the mixture was stirred for 30 minutes and then filtered. The filtrate was concentrated under reduced pressure. Manganese dioxide (13.9 g) was added to a toluene (60 mL) solution of the obtained residue, and the mixture was stirred at 60° C. for 1 hour in a nitrogen atmosphere. The reaction mixture was filtered, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (7.79 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353108B2
Source datasetuspto-grants-2016_05
ORD IDord-4b8fad8525bf411f8689b17654ad2fad
Source noteuspto-grants-2016_05