Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272462Generated: November 3, 2026

Hydrochloric Acid → Methyl 5-bromo-6-(4-fluorophenyl)-2-isopropoxynicotinate

https://huagongshe.com/reaction/2272462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromo-6-(4-fluorophenyl)-2-isopropoxynicotinonitrileHCID 117992178—
ProductMethyl 5-bromo-6-(4-fluorophenyl)-2-isopropoxynicotinateHCID 117992295—

Reaction Steps

An 8 M aqueous potassium hydroxide solution (22.1 mL) was added to a mixture of 5-bromo-6-(4-fluorophenyl)-2-isopropoxynicotinonitrile (5.92 g) and ethanol (50 mL), and the resultant mixture was stirred overnight at 100 C. The reaction mixture was neutralized with 6 M hydrochloric acid at 0 C, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. Potassium carbonate (4.88 g) and iodomethane (1.66 mL) were added to a mixture of the obtained residue and DMF (30 mL), and the mixture was stirred at 60 C for 30 minutes. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate, 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 (3.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120777B2
Source datasetuspto-grants-2015_09
ORD IDord-043e35cbbed84ccabeda16b762e9d2c5
Source noteuspto-grants-2015_09