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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963206Generated: October 30, 2026

Hydrochloric Acid → 2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one

https://huagongshe.com/reaction/963206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Tert-butyl-4,5-dichloro-2,3-dihydropyridazin-3-oneHCID 2782225—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-oneHCID 13822264—

Reaction Steps

Into 225 ml of a 3.0M diethyl ether solution of methyl magnesium bromide, 170 ml of an absolute ether solution of 74.40 g of 4,5-dichloro-2-tert-butyl-pyridazin-3-(2H)-one was dropwise added under cooling with ice at a temperature of from 5° to 10° C. After completion of the dropwise addition, the mixture was stirred at a temperature of from 5° to 10° C. for two hours. Then, 158 ml of 6N hydrochloric acid was added to the reaction solution, and then 600 ml of diethyl ether was added thereto for liquid separation. The ether layer was washed with a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography. From a fraction of n-hexane:ethyl acetate=9:1, 24.45 g of oily 2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one, was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763439
Source datasetuspto-grants-1998_06
ORD IDord-53eb1bf358dc43d68b7ea9fd2a5dbebf
Source noteuspto-grants-1998_06