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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584782Generated: November 1, 2026

1H-1,2,4-Triazole, 5-bromo-1-methyl- → 5-(7-[1,3]Dioxan-2-yl-benzofuran-5-yl)-1-methyl-1H[1,2,4]triazole

https://huagongshe.com/reaction/1584782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-Triazole, 5-bromo-1-methyl-HCID 140121—
ReactantHCID 21220869HCID 21220869—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTolueneHCID 1140—
Product5-(7-[1,3]Dioxan-2-yl-benzofuran-5-yl)-1-methyl-1H[1,2,4]triazoleHCID 2122084935.2%

Reaction Steps

A mixture of tributyl-(7-[1,3]dioxan-2-ylbenzofuran-5-yl)stannane (839 mg), 5-bromo-1-methyl-1H-[1,2,4]triazole (396 mg), bis(triphenylphosphine)palladium (II) chloride (59 mg) in dry toluene (10 ml) was heated at reflux for 42 h. The cooled solution was then filtered through Hyflo and the filtrate washed with 10% potassium fluoride solution (30 ml). The organic layer was washed with brine (30 ml), dried, and evaporated in vacuo to give a yellow oil. The crude material was purified by FCC eluting with hexane:ethyl acetate (1:1→1:3) to give the title compound as a yellow oil (171 mg,).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935972
Source datasetuspto-grants-1999_08
ORD IDord-8ae8b9a041e5485690cd599915b31973
Source noteuspto-grants-1999_08