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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726355Generated: October 31, 2026

Ethanol → HCID 23599482, compound

https://huagongshe.com/reaction/1726355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Formylphenylboronic acidHCID 2734356—
ReactantHCID 9836523HCID 9836523—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23599482HCID 23599482—

Reaction Steps

Prepared by a method analogous to that described in example 1 from (R)-N-(1-aza-bicyclo[2.2.2]oct-3-yl)(5-bromothiophene-2-carboxamide) and 3-formylphenyl boronic acid, tetrakis(triphenylphosphine)palladium(0), sodium carbonate in a mixture of tetrahydrofuran, ethanol and water. The compound was purified by reverse phase HPLC on a Waters Bondapak® C18 column using a gradient of acetonitrile and 0.1% aqueous trifluoroacetic acid as the eluent. The free base was prepared by basification of the product-containing fractions. The aqueous layer was extracted by chloroform and evaporated to gave the title compound; MS (ES+) 341 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491734B2
Source datasetuspto-grants-2009_02
ORD IDord-c9e87ed179a047cea448f51a8c75db74
Source noteuspto-grants-2009_02