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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397487Generated: October 30, 2026

1,2-Dimethoxyethane → HCID 68720623, compound

https://huagongshe.com/reaction/1397487

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% ethyl acetate in hexane, to give the title compound. MS (ESI) m/z 319 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901152B2
Source datasetuspto-grants-2014_12
ORD IDord-7561dd9083dd47dc84895322ae814496
Source noteuspto-grants-2014_12