Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194540Generated: October 31, 2026

Cesium carbonate → HCID 67009517, compound

https://huagongshe.com/reaction/2194540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2,3-Dihydro-1,4-benzodioxin-6-methylamineHCID 87102—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantHCID 11716156HCID 11716156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 67009517HCID 67009517662.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

10.6 g (37 mmol) of methyl 2-(trifluoromethylsulfonyloxy)nicotinate and 6.2 g (41 mmol) of 3,4-ethylenedioxybenzylamine were dissolved in toluene (100 mL), and 17.0 g (52 mmol) of cesium carbonate, 1.0 g (1.1 mmol) of tris(dibenzylideneacetone)dipalladium(0), and 1.3 g (5.2 mmol) of 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene were added thereto. The resulting mixture was heated and stirred for 2 hours at 80° C. The solvent was distilled off from the reaction mixture, water and ethyl acetate were added to the residue, and the resulting mixture was filtered. The filtrate was extracted with ethyl acetate, and the organic phase was washed with an aqueous solution of citric acid and water in this order, and then was dried and concentrated. The residue was purified by column chromatography (ethyl acetate:n-hexane=1:9 to 1:2), and thus 9.86 g of the title compound was obtained as an orange-colored viscous product (yield: 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334236B2
Source datasetuspto-grants-2012_12
ORD IDord-5ba362b6e4a74856a33c32a66ad166e1
Source noteuspto-grants-2012_12