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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338570Generated: October 26, 2026

Potassium Carbonate → Tert-butyl 3-(3-methylpyridin-4-yl)benzoate

https://huagongshe.com/reaction/338570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-methylpyridineHCID 2757709—
Reactant(3-((Tert-butoxy)carbonyl)phenyl)boronic acidHCID 2773299—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductTert-butyl 3-(3-methylpyridin-4-yl)benzoateHCID 5789512171.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Chloro-3-methylpyridine (2.00 g, 15.7 mmol), 3-(tert-butoxycarbonyl)phenylboronic acid (5.42 g, 24.4 mmol), a 2M aqueous solution of potassium carbonate (31.4 mL, 62.8 mmol), and palladium tetrakis(triphenylphosphine) (Pd(PPh3)4, 0.906 g, 0.784 mmol) were suspended in 1,2-dimethoxyethane (DME, 150 mL). The resulting mixture was stirred and heated to 80° C. for 60 hours. The crude reaction mixture was cooled to room temperature and then the layers were separated. The organic layer was evaporated to dryness and then purified on 120 g of silica gel utilizing a gradient of 0-70% ethyl acetate in hexanes to yield the pure product as a pale yellow oil (3.02 g, 11.2 mmol, 71.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889875B2
Source datasetuspto-grants-2014_11
ORD IDord-ad087937869e45669e753b6ee4cfb5c9
Source noteuspto-grants-2014_11