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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50101Generated: October 25, 2026

Water → HCID 178500902, compound

https://huagongshe.com/reaction/50101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-FluorobenzonitrileHCID 14517—
ReactantTin tetrachlorideHCID 24287—
ReactantMethyl 4-methyl-3-oxopentanoateHCID 2759969—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 178500902HCID 17850090281.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

22.53 g of methyl isobutyrylacetate (0.15 mol, concentration 96%) and 18.54 g of 4-fluorobenzonitrile (0.15 mol, concentration 98%) were dissolved in 150 ml of toluene and treated with 43.32 g of tin tetrachloride (0.165 mol, concentration 99%) at room temperature over the course of 12 min. After half an hour at room temperature, the mixture was heated to 80° C. After 3 h, the suspension was cooled to room temperature and treated with 150 ml of water. It was diluted with 100 ml of ethyl acetate and the phases were separated. After extraction of the aqueous phase with ethyl acetate (2×100 ml), the combined organic phases were washed with 100 ml of saturated aqueous sodium hydrogencarbonate solution, and 100 ml of 1N sodium hydroxide solution and dried over magnesium sulphate. After concentration in vacuo, 46.46 g of crude product were obtained in the form of a yellowish solid. The solid was dissolved in a mixture of 50 ml of n-hexane and 5 ml of toluene under reflux and filtered hot. The product precipitated from the filtrate on cooling. By filtering through a frit and washing the filter cake with 2×40 ml of n-hexane, 32.42 g of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate were obtained in the form of a spectroscopically pure solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710178B2
Source datasetuspto-grants-2004_03
ORD IDord-5e981c45b23e4be98159c0fce2877e2a
Source noteuspto-grants-2004_03