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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770171Generated: October 31, 2026

Ethanol → HCID 20095020, compound

https://huagongshe.com/reaction/1770171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant6-ChloronicotinamideHCID 80456—
ReactantHCID 20095048HCID 20095048—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 20095020HCID 2009502092.2%

Reaction Steps

5.00 g (20.3 mM) of 2-hexylindan-5-boronic acid, 2.79 g (17.8 mM) of 6-chloronicotinamide, 20 ml of ethanol, 30 ml of benzene, 27.9 ml of 2M-sodium carbonate aqueous solution and 1.19 g of tetrakis (triphenylphosphine) palladium (O) were mixed and heat-refluxed for 2 hours under stirring. After the reaction, the reaction mixture was poured into water to obtain an insoluble matter. The insoluble matter was recovered by filtration. Separately, the filtrate was subjected to vacuum distillation to remove the organic solvent and poured into water to obtain an insoluble matter. The insoluble matter was added to the above-prepared insoluble matter. To the resultant mixture, 100 ml of acetone was added, followed by cooling with ice to precipitate a crystal. The crystal was recovered by filtration and washed with acetone, followed by drying to obtain 5.30 g of 2-hexyl-5-(5-carbamoylpyridine-2-yl)indan (Yield: 92.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385692
Source datasetuspto-grants-1995_01
ORD IDord-abe603d5d53245598389d996423d1244
Source noteuspto-grants-1995_01