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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414208Generated: October 26, 2026

Sulfuric Acid → 4-Pyridazineethanol, 3,6-dichloro-beta,beta-dimethyl-

https://huagongshe.com/reaction/414208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantNeopentyl glycolHCID 31344—
ReactantAmmonium PersulfateHCID 62648—
Reactant3,6-DichloropyridazineHCID 67331—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
Product4-Pyridazineethanol, 3,6-dichloro-beta,beta-dimethyl-HCID 175515—

Reaction Steps

To a 5-liter flask were added 341 g. of 2,2-dimethyl-1,3-propanediol, 500 ml. of water, 223 g. of 3,6-dichloropyridazine, 100 ml. of sulfuric acid in 900 ml. of water and 51 g. of silver nitrate. To the mixture was then added, dropwise, with an insulating mantle around the flask, 600 g. of ammonium persulfate dissolved in 1 liter of water. The addition was carried out in about 20 minutes, while the temperature rose from 33° to 86°. When the addition was complete, the insulating mantle was removed and the flask was placed in a water bath to cool it. When the temperature had reached 40°, 1200 ml. of dichloromethane was added and the mixture was stirred for 10 minutes more and filtered through a polypropylene filter pad. The solids were washed with 500 ml. of dichloromethane, and the layers of the combined filtrate were separated. The aqueous layer was extracted with 1 liter of dichloromethane, and the combined organic layers were extracted with 1 liter of water, and dried over sodium sulfate. The solvent was removed under vacuum, to leave 385 g. of a gummy solid. Most of the solid was removed and dissolved in 1200 ml. of toluene at 85°. It was then cooled to 0° and filtered, and the solids were washed with cold toluene and dried under vacuum to obtain 152 g. of the desired intermediate product, 97% pure by nuclear magnetic resonance analysis, m.p. 133°-136°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791110
Source datasetuspto-grants-1988_12
ORD IDord-2eeb0a5ccb614f9180262c16038ee119
Source noteuspto-grants-1988_12