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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470676Generated: November 1, 2026

Pyridine → HCID 86720173, compound

https://huagongshe.com/reaction/1470676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-IodophenolHCID 10784—
ReactantHCID 10682881HCID 10682881—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86720173HCID 86720173—

Reaction Steps

To the suspension of the acid chloride of 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylic acid (4 mmol) obtained according to Pochet et al. (Bioorg. Med. Chem. 2000, 8, 1489) in anhydrous dioxane (10 mL) was added 2-iodophenol (5 mmol) and pyridine (0.4 mL). After 12 h stirring at room temperature, the solvent was evapotated under vacuum and the residue was suspended in methanol. The resulting precipitate was collected by filtration, washed with methanol and dried. The solid was crystallyzed in ethyl acetate (45%); mp: 156-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006466B2
Source datasetuspto-grants-2015_04
ORD IDord-536aed13fa8048088dcfd2bd56dded75
Source noteuspto-grants-2015_04