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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436083Generated: October 26, 2026

Pyridine → 3-Triphenylmethoxy-1-octyne

https://huagongshe.com/reaction/436083

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 extact 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°,δmax. (KBr) 3280 (acetylenic hydrogen), 1605, 1030, and 702 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007210
Source datasetuspto-grants-1977_02
ORD IDord-7f75aff0e2a74e5cb323650d9e819282
Source noteuspto-grants-1977_02