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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828753Generated: November 1, 2026

Propargyl alcohol → 3,3'-(Pyridine-2,6-diyl)di(prop-2-yn-1-ol)

https://huagongshe.com/reaction/1828753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant2,6-DibromopyridineHCID 12274—
CatalystHCID 178418397HCID 178418397—
SolventTriethylamineHCID 8471—
Product3,3'-(Pyridine-2,6-diyl)di(prop-2-yn-1-ol)HCID 22058386134.8%

Reaction Steps

Pd(Ph3P)4 (99 mg, 2%), CuBrSMe2 (38 mg) and propargyl alcohol (1.3 ml, 21 mmol) are added successively to a solution of 2,6-dibromopyridine (5.0 g, 21.1 mmol) in triethylamine (120 ml), and the mixture is stirred at RT for 10 min and then under reflux at 80° C. for 2 h. After cooling, the reaction mixture is filtered off through kieselguhr, and the filter cake is washed with ethyl acetate (20 ml). The organic phase is concentrated under reduced pressure. Further purification is carried out by chromatography [toluene/acetone (7:3)] on a silica gel column. This gives the title compound (2.65 g) as a colorless solid. TLC, silica gel (glass plates) [toluene/acetone (7:3)], Rf=0.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060716B2
Source datasetuspto-grants-2006_06
ORD IDord-fbc4ad8d0d0a466e84e6063d5e58290b
Source noteuspto-grants-2006_06