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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531244Generated: October 30, 2026

1,4-Dioxane → Tert-butyl 4-(5-chloro-6-methoxypyridin-3-yl)-3-methylbenzoate

https://huagongshe.com/reaction/531244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant5-Bromo-3-chloro-2-methoxypyridineHCID 40427004—
ReactantTert-butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 68937270—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Catalystpalladium(II)dichloromethaneHCID 17952575—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(5-chloro-6-methoxypyridin-3-yl)-3-methylbenzoateHCID 8668228088.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 250 mL round bottomed flask was added 5-bromo-3-chloro-2-methoxypyridine (1.5 g), tribasic potassium phosphate (2.86 g, 13.5 mmol), bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (0.275 g, 6.74 mmol), tert-butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (Step B, 2.27 g, 7.13 mmol), dioxane (50 mL) and water (3 mL). The flask was sealed and was stirred at 80° C. overnight. The reaction was cooled to room temperature, diluted with ethyl acetate, washed with water, filtered and the filtrate concentrated. The resultant residue was purified by silica gel chromatography to yield tert-butyl 4-(5-chloro-6-methoxypyridin-3-yl)-3-methylbenzoate (2.0 g, 5.99 mmol). LCMS (M+H)+: 334.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353101B2
Source datasetuspto-grants-2016_05
ORD IDord-06175ff7ad8c48c393d3c065287f95fe
Source noteuspto-grants-2016_05