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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403610Generated: November 1, 2026

Water → 6-Bromo-5-methylpyridine-3-carbaldehyde

https://huagongshe.com/reaction/2403610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-FormylmorpholineHCID 20417—
Reactant2,5-Dibromo-3-methylpyridineHCID 817680—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-5-methylpyridine-3-carbaldehydeHCID 4475488471.2%

Reaction Steps

Under an argon atmosphere, a solution of 2 M isopropylmagnesium chloride in THF (5.5 ml) was cooled to −78° C., and a solution of 2,5-dibromo-3-methylpyridine (2.5 g) in THF (10 ml) was added dropwise. After stirring at the same temperature for 30 minutes, a solution of morpholine-4-carboaldehyde (1.26 g) in THF (5 ml) was added dropwise thereto, followed by elevating the temperature to 0° C. over 30 minutes, followed by stirring at 0° C. for 2 hours. To the reaction mixture was added water, followed by extraction with EtOAc. The organic layer was dried over Na2SO4 and the solvent was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain 6-bromo-5-methyl nicotine aldehyde (1.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-978362908f82470696915ce19fc85495
Source noteuspto-grants-2014_08