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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29367Generated: October 26, 2026

1,2-Dimethoxyethane → 3-Methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/29367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl esterHCID 86599030—
SolventWaterHCID 962—
Product3-Methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl esterHCID 6871636374.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl ester (258 mg, 0.68 mmol) was mixed with K2CO3 (207 mg, 2.2 eq), pyridine-4-boronic acid (110 mg, 1.3 eq), Pd(Ph3)4 (43 mg, 0.05 eq), 3 mL of 1,2-dimethoxyethane and 0.5 mL of water. The mixture was heated and stirred in an 85° C. oil bath for 5 h. The reaction mixture was poured into water and was extracted with ethyl acetate. The organic extract was washed with water and dried over sodium sulfate. Removal of solvent gave the crude product, which was purified by column chromatography to give 156 mg of 3-methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester, obtained as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-b31709faa8774b43adaf6d01d013a3d2
Source noteuspto-grants-2008_09