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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814487Generated: October 31, 2026

3-Bromopyridine → 3-Bromopyridine-4-carboxaldehyde

https://huagongshe.com/reaction/1814487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
ReactantN-FormylmorpholineHCID 20417—
ReactantAmmonium ChlorideHCID 25517—
ReactantLDA cyclohexaneHCID 86604122—
SolventTetrahydrofuranHCID 8028—
Product3-Bromopyridine-4-carboxaldehydeHCID 276299740%

Reaction Steps

3-Bromopyridine (1.582 g) was dissolved in tetrahydrofuran (20 ml), followed by the addition of a 1.5M solution of lithium diisopropylamide/cyclohexane (7.3 ml) in nitrogen atmosphere at −70° C., and the resulting mixture was stirred for 5 min. Continuously, 4-formylmorpholine (3 ml) was added thereto and stirred for 20 min, followed by the further stirring at room temperature for 30 min. An aqueous solution of saturated ammonium chloride was added to the reaction mixture, and then it was extracted with ethyl acetate. The resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a colorless solid (749 mg, yield; 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-4008616c772c4d3c85b759cc7f1eac4e
Source noteuspto-grants-2005_04