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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363164Generated: November 1, 2026

1,2-Dimethoxyethane → HCID 67111294, compound

https://huagongshe.com/reaction/2363164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantCesium carbonateHCID 10796—
Reactant3-Isopropylbenzeneboronic acidHCID 2773478—
ReactantHCID 67238529HCID 67238529—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 67111294HCID 6711129477%

Reaction Steps

In a 5 ml glass tube were placed 5-bromo-thiophene-2-carboxylic acid [1-(3,5-difluoro-4-methanesulfonylamino-phenyl)-ethyl]-amide (50 mg, 0.12 mmol), 3-isopropyl phenyl boronic acid (37 mg, 0.23 mmol), Cs2CO3 (114 mg, 0.34 mmol), Pd(PPh3)2Cl2 (6.4 mg, 0.009 mmol), DME (0.8 mL), ethanol (0.2 mL), and a magnetic stir bar. The vial was sealed with septum and placed into the Microwave cavity. The vial was irradiated in a Microwave synthesizer at 140° C. for 20 min. The mixture was diluted with EtOAc and washed with 1N HCl and water. The organic layer was dried over anhydrous MgSO4 and concentrated under reduced pressure. The crude residue was purified by column chromatography (gradient 12% to 100% EtOAc in n-hexane) to give title compound (42 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691855B2
Source datasetuspto-grants-2014_04
ORD IDord-ed58e750fd3d4bb286823af892ad1a67
Source noteuspto-grants-2014_04