Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272464Generated: October 31, 2026

Tetrahydrofuran → 5-Cyclopropyl-6-(4-fluorophenyl)-2-isopropoxynicotinaldehyde

https://huagongshe.com/reaction/2272464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 5-cyclopropyl-6-(4-fluorophenyl)-2-isopropoxynicotinateHCID 117992411—
SolventWaterHCID 962—
Product5-Cyclopropyl-6-(4-fluorophenyl)-2-isopropoxynicotinaldehydeHCID 11799216985%

Reaction Steps

A THF (20 mL) solution of methyl 5-cyclopropyl-6-(4-fluorophenyl)-2-isopropoxynicotinate (3.17 g) was added to a THF (20 mL) suspension of lithium aluminum hydride (365 mg) under ice cooling in a nitrogen atmosphere. After stirring at the same temperature as above for 30 minutes, water (0.35 mL) and a 15% aqueous sodium hydroxide solution (0.35 mL) were added thereto, and the mixture was stirred for 5 minutes. Then, water (1.05 mL) was further added thereto. The reaction mixture was stirred for 30 minutes and then filtered. The filtrate was concentrated under reduced pressure. Manganese dioxide (8.36 g) was added to a toluene (30 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 (2.45 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120777B2
Source datasetuspto-grants-2015_09
ORD IDord-6a184f7cadbd4094bc128281624ccb05
Source noteuspto-grants-2015_09