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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465575Generated: October 30, 2026

Diethylamine → HCID 11779758, compound

https://huagongshe.com/reaction/465575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
Reactant3-BromopyridineHCID 12286—
ReactantHCID 10353657HCID 10353657—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
ProductHCID 11779758HCID 11779758—

Reaction Steps

A mixture of 5.84 g (25.8 mmol) 4-hydroxy-8-(2-tetrahydropyranyloxy)-1-octyne, 4.7 ml diethylamine, 10 ml (100 mmol) 3-bromopyridine, 0.032 g copper (I) iodide, and 0.187 g bis-triphenylphosphine palladium (II) chloride is stirred at room temperature for 18 h. The solvent is evaporated and the residue taken up in ether. The ether layer is washed with saturated aqueous sodium bicarbonate, water, brine, dried, filtered and evaporated to get an amber oil which is purified by chromatography using ether as the eluent to give 1-(3-pyridyl)-4-hydroxy-8-(2-tetrahydropyranyloxy)-1-octyne; NMR (CDCl3): delta 4.6 (brs,1H), 2.6 (d,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153214
Source datasetuspto-grants-1992_10
ORD IDord-3fbac1e2adce4b2abd6d8533df5e20ef
Source noteuspto-grants-1992_10