Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50109Generated: October 26, 2026

Water → HCID 178500884, compound

https://huagongshe.com/reaction/50109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutyronitrileHCID 6559—
ReactantTin tetrachlorideHCID 24287—
ReactantMethyl 4-fluorobenzoylacetateHCID 579425—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 178500884HCID 17850088418,998.801%

Reaction Conditions

Temperature80 °C

Reaction Steps

39.2 g of methyl 4-fluorobenzoylacetate (0.20 mmol) and 16.8 g of isobutyronitrile (0.24 mol, concentration >99%) were dissolved in 200 ml of toluene and treated with 57.9 g of tin tetrachloride (0.22 mmol, concentration >99%) at room temperature after the course of 10 minutes. After 30 min at room temperature, the mixture was heated to 80° C. After 8 h, the suspension was again cooled to room temperature and treated with 200 ml of water. The mixture was diluted with 200 ml of ethyl acetate and the phases were separated. The organic phase was washed twice with 40 ml of 1N sodium hydroxide solution and concentrated in vacuo (40° C./25 mbar) after drying over magnesium sulphate. 50.9 g of crude product were obtained in the form of a yellow oil. After chromatography of 12.0 g of crude product on silica gel (eluent: hexane/isopropanol 90:10), 10.08 g of methyl 3-amino-2-[1-(4-fluorophenyl)methanoyl]-4-methylpent-2-enoate were obtained in the form of a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710178B2
Source datasetuspto-grants-2004_03
ORD IDord-f6367908ef1d44ed8015b73da1427da5
Source noteuspto-grants-2004_03