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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888397Generated: October 29, 2026

Diisopropylamine → Methyl 3-isopropenyl-5-(5-methylpyridin-2-yl)benzoate

https://huagongshe.com/reaction/888397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
ReactantMethyl 3-bromo-5-(5-methylpyridin-2-yl)benzoateHCID 59599704—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-isopropenyl-5-(5-methylpyridin-2-yl)benzoateHCID 6850035998.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 3-bromo-5-(5-methylpyridin-2-yl)benzoate (1.00 g, 3.27 mmol) in N,N-dimethylformamide (9.80 mL) and water (3.27 mL) was 2-isopropenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.921 mL, 4.90 mmol), palladium(II) acetate (37.0 mg, 0.163 mmol), 3,3′3″-phosphinidynetris(benzenesulfonic acid)trisodium salt (278 mg, 0.490 mmol) and diisopropylamine (1.16 mL, 8.17 mmol) and the mixture was heated to 80° C. After 50 min, the reaction was allowed to cool to ambient temperature and filtered. Purification by reverse phase chromatography (C-18, 90% water/acetonitrile→40% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (864 mg). MS 268.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-195a0940c91e44b29ac8d50b1d12a004
Source noteuspto-grants-2012_08