Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199135Generated: October 30, 2026

Sulfuric Acid → [3,5-Dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-ylmethyl)-phenyl]-acetonitrile

https://huagongshe.com/reaction/2199135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium CyanideHCID 8929—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(4-Bromomethyl-2,6-dichloro-benzyl)-4-isopropyl-pyridazin-3-oneHCID 59834446—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product[3,5-Dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-ylmethyl)-phenyl]-acetonitrileHCID 59834478—

Reaction Steps

A suspension of sodium cyanide (270 mg, 5.51 mmol) in dimethyl sulfoxide (2 mL) at room temperature was treated with concentrated sulfuric acid (0.1 mL, 1.88 mmol) and a solution of 6-(4-bromomethyl-2,6-dichloro-benzyl)-4-isopropyl-pyridazin-3-one (54) (70 mg, 0.180 mmol) in dimethyl sulfoxide (2 mL). The reaction mixture was stirred at room temperature for 30 min and then at 50° C. for 1 h. The reaction was cooled to room temperature, poured into a saturated aqueous sodium bicarbonate solution (50 mL), was diluted with water (20 mL) and then extracted with ethyl acetate (3×75 mL). The organic layers were combined and washed with a saturated aqueous sodium chloride solution (50 mL), dried over magnesium sulfate, filtered, and concentrated under vacuum. The resulting oil was dried under high vacuum to afford [3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-ylmethyl)-phenyl]-acetonitrile (55) as an orange oil (assume 0.180 mmol) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE046024E1
Source datasetuspto-grants-2016_06
ORD IDord-ff4aeaaf534d45caab369455b56a6c39
Source noteuspto-grants-2016_06