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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909443Generated: October 28, 2026

Pyridine → HCID 58712145, compound

https://huagongshe.com/reaction/1909443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHCID 58712184HCID 58712184—
CatalystPiperidineHCID 8082—
SolventEthyl AcetateHCID 8857—
ProductHCID 58712145HCID 58712145—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 1-(5-ethyl-2,4-dihydroxy-phenyl)-2-naphthalen-2-yl-ethanone (c, 0.50 g) was added a mixture of pyridine (2 mL), trimethyl orthoformate (2 mL) and piperidine (2 drops), and the mixture was heated at 120° C. for 12 h. The mixture was cooled to room temperature, diluted with EtOAc (100 mL) then washed with 1 N HCl (100 mL). The organic layer was washed with water and dried. The oil obtained on concentration of the organic layer was crystallized in EtOAc/hexanes to give 6-ethyl-7-hydroxy-3-naphthalen-2-yl-chromen-4-one (d, 0.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598366B2
Source datasetuspto-grants-2013_12
ORD IDord-d589ea03042e415d9b70f3a402cf96b0
Source noteuspto-grants-2013_12