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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673019Generated: October 29, 2026

1,2-Dimethoxyethane → HCID 15947801, compound

https://huagongshe.com/reaction/1673019

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
ReactantEthyl 1-(4-bromo-2-chlorophenyl)-2-(2,6-dichlorophenyl)-1H-imidazole-4-carboxylateHCID 59240404—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 15947801HCID 1594780179%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 2 L round bottom flask attached with condenser column and magnetic stir bar was added 1-(4-Bromo-2-chloro-phenyl)-2-(2,6-dichloro-phenyl)-1H-imidazole-4-carboxylic acid ethyl ester (21.1 g, 44.5 mmol), 3-methylsulfonylphenyl boronic acid (9.78 g, 48.9 mmol), PdCl2dppf (1.09 g, 3 mol %), K2CO3 (18.9 g, 137 mmol), 1,2-dimethoxyethane (250 mL) and H2O (50 mL). The reaction solution was allowed to stir at 80° C. for 2.5 hrs. The reaction solution was diluted with EtOAc (150 mL) and filtered through a Celite padded Buchner funnel to remove spent Pd. The filtrate was transferred to a separatory funnel and washed with aq NH4Cl (300 mL) and aq NaCl (200 mL). The organic phase was dried over Na2SO4, filtered, concentrated on the rotavapor and chromatographed through a 300 g SiO2 column using a mobile phase gradient of 3% EtOAc to 100% EtOAc to afford 19.3 g (79% yield) of the title compound. MS (ESI) 549.3, 551.3, 553.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998995B2
Source datasetuspto-grants-2011_08
ORD IDord-6a5cb4977c2b4ed09537eab6db91c0b3
Source noteuspto-grants-2011_08