Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860654Generated: November 2, 2026

Ethanol → Ethyl 4-(3-fluoro-4-methylphenyl)-3,3-dimethylbutanoate

https://huagongshe.com/reaction/1860654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant4-(3-Fluoro-4-methylphenyl)-3,3-dimethylbutanalHCID 18624188—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
ProductEthyl 4-(3-fluoro-4-methylphenyl)-3,3-dimethylbutanoateHCID 18624144—

Reaction Steps

A solution of silver nitrate (5.76 g, 33.9 mmol) in 20 ml H2O was added to a solution of the product of STEP 4 (3.8 g, 16.9 mmol) in 80 ml ethanol. A solution of Sodium hydroxide (2.71 g, 67.7 mmol) in 10 ml H2O was added dropwise at room temperature. After 2 h, the reaction was filtered through a short column of Celite®. The filtrate was diluted with H2O and extracted with ether (3×30 ml). The aqueous layer was acidified with concentrated HCl and extracted with chloroform. Chloroform layer was dried with MgSO4 and concentrated. The residue was dissolved in 50 ml ethanol and 25 ml 4N HCl/dioxane solution. It was stirred at room temperature for 60 h and then concentrated to afford a colorless oil in 4.14 g. NMR spectra of the product were consistent for the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531494B1
Source datasetuspto-grants-2003_03
ORD IDord-03c92f72996d429986b0db168b68917a
Source noteuspto-grants-2003_03