Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29356Generated: October 27, 2026

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

https://huagongshe.com/reaction/29356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl esterHCID 86599030—
CatalystWaterHCID 962—
SolventWaterHCID 962—
Product3-Methyl-4-phenyl-benzofuran-2-carboxylic acid tert-butyl esterHCID 6871289377%

Reaction Conditions

Temperature85 °C

Reaction Steps

3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl ester (85 mg, 0.25 mmol) was mixed with K2CO3 (68 mg, 0.5 mmol), phenylboronic acid (31 mg, 0.25 mmol), Pd(Ph3)4 (14 mg, 0.01 mmol), 1 mL of 1,2-dimethoxyethane and 2 drops of water. The mixture was heated and stirred in an 85° C. oil bath for 2 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. Filtration followed by removal of the solvent in vacuo gave the crude product (71 mg), which was purified by column chromatography to give 53 mg (77% yield) of 3-methyl-4-phenyl-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-e097fe578d814ac1a945e082a61e03c5
Source noteuspto-grants-2008_09