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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399559Generated: October 26, 2026

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

https://huagongshe.com/reaction/1399559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPhenylboronic AcidHCID 66827—
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 8666564566.1%

Reaction Steps

To a suspension of methyl 2-(2,4-dichloro-6-methylpyrimidin-5-yl)acetate (4.42 g; 18.80 mmol) in a mixture of degassed DME (75 mL) and water (25 mL) was added phenyl boronic acid (5.73 g; 47 mmol), Tetrakis(triphenylphosphine) palladium(0) (2 g; 1.731 mmol) and diisopropyl ethylamine (12.96 mL; 75 mmol). The reaction was stirred under reflux for 3.5 h. The reaction mixture was 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 over 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 3.44 g (65%) of the title compound as a white solid. ESI/APCI(+): 277 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-a6d5a5b1e1ea46c59d108181722b0863
Source noteuspto-grants-2014_12