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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352022Generated: November 1, 2026

Water → 2-t-butyl-5-(alpha-ethyl-p-t-butylbenzylthio)-4-methyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/2352022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-t-butyl-5-mercapto-4-methyl-3(2H)-pyridazinoneHCID 13822265—
Reactant1-(tert-Butyl)-4-(1-chloropropyl)benzeneHCID 14674267—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-t-butyl-5-(alpha-ethyl-p-t-butylbenzylthio)-4-methyl-3(2H)-pyridazinoneHCID 1382512553.7%

Reaction Steps

To a solution of 0.8 g (0.004 mol) of 2-t-butyl-5-mercapto-4-methyl-3(2H)-pyridazinone and 0.84 g (0.004 mol) of α-ethyl-p-t-butylbenzyl chloride dissolved in 20 ml of N,N-dimethylformamide was added 1.0 g (0.01 mol) of sodium carbonate at room temperature under stirring. After addition, the resulting mixture was stirred at 70°~80° C. for four hours. After allowed to cool, the reaction mixture was poured into 200 ml of water and then extracted with 100 ml of benzene. The resulting benzene layer was washed with 100 ml of water, dried over anhydrous sodium sulfate, and freed of solvent by distillation to give 1.5 g of crude product. The crude product was fractionated on silica gel column chromatography [developer: a mixed solvent of benzene and ethyl acetate (10:1 mixture)] to obtain 0.8 g of 2-t-butyl-5-(α-ethyl-p-t-butylbenzylthio)-4-methyl-3(2H)-pyridazinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874861
Source datasetuspto-grants-1989_10
ORD IDord-9e97fee86de24cd3bfa400bc7b22559a
Source noteuspto-grants-1989_10