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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399683Generated: October 30, 2026

Dichloromethane → Methyl 2-(4-benzyl-6-methyl-2-phenylpyrimidin-5-yl)pentanoate

https://huagongshe.com/reaction/1399683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethyl 2-(4-chloro-6-methyl-2-phenylpyrimidin-5-yl)pentanoateHCID 86665652—
ReactantHCID 178418336HCID 178418336—
ReactantHCID 178528066HCID 178528066—
CatalystZincchlorideHCID 3007855—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4-benzyl-6-methyl-2-phenylpyrimidin-5-yl)pentanoateHCID 5099499581%

Reaction Steps

To a cooled (0° C.) solution of anhydrous zinc chloride (0.060 mg; 0.439 mmol) in tetrahydrofuran (0.8 mL) under nitrogen atmosphere was added dropwise a benzylmagnesium chloride solution (1M in THF) (0.408 mL; 0.408 mmol). After 15 min, the solution was allowed to warm up to room temperature for 10 min. To an argon purged reaction tube was added methyl 2-(4-chloro-6-methyl-2-phenylpyrimidin-5-yl)pentanoate (0.100 g; 0.314 mmol), (1,1′-Bis(diphenylphosphino)ferrocene)-dichloropalladium(II) complex with dichloromethane (0.015 g; 0.022 mmol) and tetrahydrofuran (3 mL). The milky benzylzinc solution was added dropwise, the mixture was stirred at room temperature for 30 min and then heated at 65° C. for 20 h. The reaction mixture was diluted with water and extracted twice with ethyl acetate. The combined organics were washed with a solution of ethylenediaminetetraacetic acid, water, brine, dried over magnesium sulphate, filtered and concentrated under reduced pressure. Purification by flash-chromatography on silica gel using a gradient of ethyl acetate (2-20%) in heptane furnished 0.095 g (81%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-789809e2357a4717ac63d8427475968c
Source noteuspto-grants-2014_12