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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885115Generated: October 30, 2026

1,2-Dimethoxyethane → HCID 68720623, compound

https://huagongshe.com/reaction/885115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantCesium fluorideHCID 25953—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
ReactantHCID 68721618HCID 68721618—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
ProductHCID 68720623HCID 68720623—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of Example 24A (0.750 g, 2/04 mmol), CsF (0.930 g, 6.12 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (0.447 g, 2.04 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.231 g, 0.200 mmol) in a solvent mixture of dimethoxyethane (5 mL) and methanol (5 mL) was heated to 90° C. for 16 h. The reaction was cooled to room temperature and partitioned between H2O (10 mL) and ethyl acetate (10 mL). The layers were separated, and the aqueous was extracted with additional ethyl acetate (2×10 mL). The combined organics were dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by chromatography on SiO2 gel, eluting with a gradient of 10% ethyl acetate in hexane to 50% ethylacetate in hexane, to give the title compound. MS (ESI) m/z 319 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242139B2
Source datasetuspto-grants-2012_08
ORD IDord-393bdaa6e4e84442b484155fa6d5416a
Source noteuspto-grants-2012_08