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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605784Generated: October 31, 2026

Pyridine → 1,1',1''-{[(Hex-5-yn-3-yl)oxy]methanetriyl}tribenzene

https://huagongshe.com/reaction/1605784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrityl chlorideHCID 6456—
Reactant5-Hexyn-3-olHCID 89223—
SolventWaterHCID 962—
Product1,1',1''-{[(Hex-5-yn-3-yl)oxy]methanetriyl}tribenzeneHCID 20565106—

Reaction Steps

A stirred solution of 9.81 g. (0.10 moles) of 4-hydroxy-1-hexyne and 33.5 g. (0.12 moles) of triphenylmethyl chloride in 100 ml. of dry pyridine is heated at reflux for 2 hours. The cooled mixture is treated with water and extracted with a hexane-ether mixture. The extract is washed successively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. Column chromatography of the residue on Florisil gives an oil, ν max. 3290 (acetylenic hydrogen), 1600, 1030, and 705 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950406
Source datasetuspto-grants-1976_04
ORD IDord-536689a011784a73bcf8974105eb7f5e
Source noteuspto-grants-1976_04