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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524920Generated: October 30, 2026

2-(2-Methyl-1,3-dioxolan-2-yl)acetaldehyde → 3-bromo-4-(5-methyl-1H-pyrazol-1-yl)-5-nitropyridine

https://huagongshe.com/reaction/524920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Methyl-1,3-dioxolan-2-yl)acetaldehydeHCID 11007926—
Reactant3-Bromo-4-hydrazinyl-5-nitropyridineHCID 86720974—
SolventEthanolHCID 702—
Product3-bromo-4-(5-methyl-1H-pyrazol-1-yl)-5-nitropyridineHCID 86720975—

Reaction Steps

2-(2-methyl-1,3-dioxolan-2-yl)acetaldehyde (320 mg, 2.459 mmol) and (3-bromo-5-nitro-4-pyridyl)hydrazine (286.4 mg, 1.229 mmol) were heated under reflux in ethanol (2.864 mL) overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between DCM and a saturated aqueous sodium hydrogen carbonate solution. Combined organic extract was dried over MgSO4 and concentrated in vacuo to leave 3-bromo-4-(5-methyl-1H-pyrazol-1-yl)-5-nitropyridine as a yellow oil. (200 mg, 85%). MS (ES+) 284.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-28d38fbbce2f4f7fbd1058e1a32f35c4
Source noteuspto-grants-2016_05