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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732501Generated: October 31, 2026

Pyridine → 3-Triphenylmethoxy-1-octyne

https://huagongshe.com/reaction/1732501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromotriphenylmethaneHCID 11692—
Reactant1-Octyn-3-olHCID 13166—
ReactantPotassium BromideHCID 253877—
SolventWaterHCID 962—
Product3-Triphenylmethoxy-1-octyneHCID 12675347—

Reaction Steps

A mixture of 1.26 g. (10.0 mmoles) of 1-octyn-3-ol, 4.85 g. (15.0 mmoles) of triphenylmethyl bromide, and 50 ml. of dry pyridine is heated at 95° C. for 60 minutes with occasional swirling. The solution is cooled, treated with water, and extracted with ether. The extract is washed successively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The crude product is purified by chromatography on Florisil and recrystallization from petroleum ether to give white crystals, m.p. 65°-66.5°, νmax. (KBr) 3280 (acetylenic hydrogen), 1605, 1030, and 702 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237316
Source datasetuspto-grants-1980_12
ORD IDord-6e7b7974b32e4a2cbe6a97a7cd7ed3d9
Source noteuspto-grants-1980_12