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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291353Generated: November 1, 2026

Pyridine → HCID 14988330, compound

https://huagongshe.com/reaction/2291353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2H-Pyran, tetrahydro-2-(4-iodophenoxy)-HCID 2916803—
Catalyst99522-35-7HCID 14827470—
SolventWaterHCID 962—
ProductHCID 14988330HCID 14988330—

Reaction Steps

20 Grams of p-tetrahydropyranyloxyiodobenzene and 70 ml of anhydrous pyridine containing 11.3 g of copper (I) 3-acetyloxy-1-propyn-1-ide were refluxed for 6 hours under an atmosphere of argon gas. After the reaction was completed the reaction mixture was poured into water and the whole mixture was extracted with chloroform. The chloroform layer was washed with water, dried and the solvent was removed by evaporation. The residue thus obtained was purified by means of a silica gel column chromatography (eluent: chlorofrom:n-hexane=1:1) to yield 8 g of 4-[4-(2-tetrahydropyranyloxy)phenyl]-3-butynyl acetate in the form of colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04795814
Source datasetuspto-grants-1989_01
ORD IDord-d5ab9467131b4cc0bce4f5d9379c758a
Source noteuspto-grants-1989_01