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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294523Generated: October 30, 2026

Acetyl bromide → 4-Bromo-6-methylpyridazine 1-oxide

https://huagongshe.com/reaction/1294523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
ReactantSodium HydroxideHCID 14798—
Reactant6-Methyl-4-nitro-pyridazine-1-oxideHCID 14792118—
SolventAcetic AcidHCID 176—
Product4-Bromo-6-methylpyridazine 1-oxideHCID 66858920—

Reaction Steps

6-Methyl-4-nitro-pyridazine-1-oxide (270 mg, 1.74 mmol) was dissolved in 2 mL acetic acid, acetyl bromide (650 mL, 8.7 mmol) was added and the reaction mixture was heated at reflux for 1 h. The reaction mixture was poured into crushed ice, the mixture was neutralized by addition of sodium hydroxide and extracted three times with dichloromethane (50 mL each). The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel (heptane/ethyl acetate 80:20->30:70 gradient) and the desired product was obtained as a light brown solid (150 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241760B2
Source datasetuspto-grants-2007_07
ORD IDord-9b02ca2beffd4715aa2613f6653c33f5
Source noteuspto-grants-2007_07