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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207113Generated: October 29, 2026

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

https://huagongshe.com/reaction/2207113

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 86682280—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 250 mL RBF 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 (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 concentrated. The resultant residue was purified by column chromatography to yield tert-butyl 4-(5-chloro-6-methoxypyridin-3-yl)-3-methylbenzoate. MS ESI calc'd. for C18H21ClNO3 [M+H]+ 334.1. found 334.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376408B2
Source datasetuspto-grants-2016_06
ORD IDord-28b0ef2fb79546d484eaa4d729891eba
Source noteuspto-grants-2016_06