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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055023Generated: October 26, 2026

Pyridine → HCID 84671998, compound

https://huagongshe.com/reaction/1055023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant1-(3-Bromo-1-methyl-1H-1,2,4-triazol-5-YL)ethan-1-OLHCID 90017669—
SolventDichloromethaneHCID 6344—
ProductHCID 84671998HCID 8467199858.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-(3-bromo-1-methyl-1H-1,2,4-triazol-5-yl)ethanol (1.639 g, 7.95 mmol, Eq: 1.00) and pyridine (944 mg, 965 μl, 11.9 mmol, Eq: 1.5) in dichloromethane (237 ml) was cooled to 0° C. then Dess-Martin periodinane (15% in dichloromethane, 24.7 g, 8.75 mmol, Eq: 1.1) was added. The resulting mixture was stirred for 4 hours at 0° C. under nitrogen atmosphere. The mixture was diluted with dichloromethane and washed with sat. sodium hydrogen carbonate. The organic layer was separated, dried over magnesium sulfate, filtrated and evaporated. The crude material was applied on silica gel and purified by flash chromatography over a 20 g silica gel column using dichloromethane/methanol 0-3% & 5% NH3 as eluent affording 1-(5-bromo-2-methyl-2H-[1,2,4]triazol-3-yl)-ethanone (948 mg, 58.4%) as a white solid. MS: m/z=203 (EI)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394311B2
Source datasetuspto-grants-2016_07
ORD IDord-0d9657c11442411ab611afac4dc96f33
Source noteuspto-grants-2016_07