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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69145Generated: October 26, 2026

tert-Butanol → 7-Fluoroimidazo[1,2-a]pyridine-6-carbaldehyde

https://huagongshe.com/reaction/69145

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant2,6-LutidineHCID 7937—
ReactantSodium periodateHCID 23667635—
Reactant7-Fluoro-6-vinyl-imidazo[1,2-a]pyridineHCID 57917482—
CatalystOsmiumHCID 23937—
SolventSodium BicarbonateHCID 516892—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product7-Fluoroimidazo[1,2-a]pyridine-6-carbaldehydeHCID 57917443—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 7-fluoro-6-vinyl-imidazo[1,2-a]pyridine (xv) (94 mg, 0.58 mmol), sodium periodate (496 mg, 2.32 mmol) and 2,6-lutidine (0.135 mL, 1.16 mmol) in dioxane/water 3:1 (4.8 mL) was added in two portions a 2.5% solution of osmium tetroxyde in tert-butanol (2×0.728 mL, 2×0.058 mmol). The RM was stirred at rt for 19.5 h and at 50° C. for 24 h. The RM was diluted with aqueous saturated NaHCO3 and extracted twice with EtOAc. The organic layers were washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by chromatography with DCM and MeOH to yield the title product as a brown solid (TLC RF (DCM/MeOH 9: 1)=0.40, MH+=165).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-0cef86927abf407b9d0afff550992f00
Source noteuspto-grants-2014_09