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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461269Generated: October 25, 2026

Pyridine → 4-Triphenylmethoxy-1-Octyne

https://huagongshe.com/reaction/461269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromotriphenylmethaneHCID 11692—
Reactant1-Octyn-4-olHCID 103656—
SolventWaterHCID 962—
Product4-Triphenylmethoxy-1-OctyneHCID 12786165—

Reaction Steps

A mixture of 10 g. (0.08 moles) of 4-hydroxy-1-octyne [L. Crombie and A. G. Jacklin, J. Chem. Soc., 1632 (1957)] and 30.75 g. (0.09 moles) of triphenylmethyl bromide in 85 ml. of dry pyridine is heated on the steam bath for 2 hours. The cooled mixture is treated with water and extracted with ether. The extract is washed successively with ice cold 2% hydrochloric acid, saturated sodium chloride solution, dried with magnesium sulfate, and taken to dryness. Column chromatography of the residue on Florisil affords an oil; λ max 3.01, 4.72 (acetylenic hydrogen), 6.28 9.65 and 14.25 μ (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061672
Source datasetuspto-grants-1977_12
ORD IDord-5e40d2260646445ab311d47721894684
Source noteuspto-grants-1977_12