Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087140Generated: October 31, 2026

Pyridine → HCID 14988330, compound

https://huagongshe.com/reaction/1087140

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 finished 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: chloroform: 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 numberUS05034395
Source datasetuspto-grants-1991_07
ORD IDord-ece6df06392f4cd5a468e93bcb3eff94
Source noteuspto-grants-1991_07