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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419942Generated: November 1, 2026

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

https://huagongshe.com/reaction/2419942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrityl chlorideHCID 6456—
Reactant5-Hexyn-3-olHCID 89223—
ReactantHCID 178461831HCID 178461831—
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 successsively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. Column chromatography of the residue on Florisil gives an oil, λ mas. 3290 (acetylene hydrogen), 1600, 1030 and 705 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107441
Source datasetuspto-grants-1978_08
ORD IDord-2733a1b946d9494c875f66e1ed906534
Source noteuspto-grants-1978_08