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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399561Generated: October 25, 2026

1,2-Dimethoxyethane → Methyl 2-(2-chloro-4-methyl-6-phenylpyrimidin-5-yl)acetate

https://huagongshe.com/reaction/1399561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantTolylboronic acidHCID 79799—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-(2,4-dichloro-6-methylpyrimidin-5-yl)acetateHCID 19044674—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
ProductMethyl 2-(2-chloro-4-methyl-6-phenylpyrimidin-5-yl)acetateHCID 8666564581.1%

Reaction Steps

To a suspension of methyl 2-(2,4-dichloro-6-methylpyrimidin-5-yl)acetate (4 g; 17.02 mmol) in a mixture of degassed DME (75 mL) and water (25 mL) was added p-tolylboronic acid (4.63 g; 34 mmol), Tetrakis(triphenylphosphine) palladium(0) (2 g; 1.731 mmol) and diisopropyl ethylamine (11.73 mL; 68.1 mmol). The reaction was stirred under reflux for 3.5 h. The reaction mixture was then partitioned between brine and ethyl acetate. The phases were separated and the water layer was extracted with ethyl acetate. The combined organic layers were dried with magnesium sulphate and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel using a linear gradient of ethylacetate (5-40%) in heptane to give 3.82 g (61%) of the title compound as a white solid (purity: 80%). ESI/APCI(+): 291 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-ed14b3a07a9544b097d214f1dd3b5c38
Source noteuspto-grants-2014_12