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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127053Generated: October 31, 2026

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

https://huagongshe.com/reaction/127053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrityl chlorideHCID 6456—
Reactant5-Hexyn-3-olHCID 89223—
SolventPyridineHCID 1049—
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, max. 3290 (acetylenic hydrogen), 1600, 1030 and 705 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254285
Source datasetuspto-grants-1981_03
ORD IDord-cf4f0c31f49e4640a2294844a8c01928
Source noteuspto-grants-1981_03