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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50108Generated: October 25, 2026

Water → HCID 178500884, compound

https://huagongshe.com/reaction/50108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutyronitrileHCID 6559—
ReactantTin tetrachlorideHCID 24287—
ReactantMethyl 4-fluorobenzoylacetateHCID 579425—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 178500884HCID 17850088459.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

5.00 g of methyl 4-fluorobenzoylacetate (24.2 mmol, concentration 95%) and 1.69 g of isobutyronitrile (24.2 mmol, concentration 98%) were dissolved in 25 ml of toluene and treated with 7.01 g of tin tetrachloride (26.6 mmol, concentration >99%) at room temperature after the course of 10 minutes. After 3 h at room temperature, the mixture was heated to 80° C. After 11.5 h, the suspension was again cooled to room temperature and treated with 25 ml of water. The mixture was diluted with 10 ml of ethyl acetate and the phases were separated. The organic phase was washed twice with 10 ml of 1N sodium hydroxide solution and concentrated in vacuo (40° C./25 mbar) after drying over magnesium sulphate. 6.18 g of crude product were obtained in the form of a yellow oil. After chromatography on silica gel (eluent: hexane/ethyl acetate 1.5:1), 3.84 g of methyl 3-amino-2-[1-(4-fluorophenyl)methanoyl]-4-methylpent-2-enoate were obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710178B2
Source datasetuspto-grants-2004_03
ORD IDord-4d1657614f474eed850a97ba398cdfb1
Source noteuspto-grants-2004_03