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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352525Generated: October 30, 2026

Benzene → HCID 13648702, compound

https://huagongshe.com/reaction/2352525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chlorobenzyl mercaptanHCID 80409—
Reactant2-Tert-butyl-4,5-dichloro-2,3-dihydropyridazin-3-oneHCID 2782225—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
ProductHCID 13648702HCID 1364870264.4%

Reaction Steps

Sodium hydroxide 0.7 g was dissolved in 15 ml of water, and thereto were added 100 ml of benzene, 3.3 g of 2-tert.-butyl-4,5-dichloro-3(2H)-pyridazinone and 0.15 g of triethylbenzylammonium chloride. The resulting solution was incorporated with 2.4 g of 4-chlorobenzyl mercaptan at room temperature and then stirred for 15 hours. After completion of the reaction, only the organic layer was separated therefrom, washed with a 5% aqueous solution of sodium hydroxide and then with water, and dried over anhydrous sodium sulfate. Solvent was distilled away therefrom under reduced pressure. The resulting oily residue was incorporated with hexane to give crystals. The crystals were filtered off to obtain 3.3 g of the intended compound (yield: 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877787
Source datasetuspto-grants-1989_10
ORD IDord-9eff4ec39d5149b4a86c742d50517c75
Source noteuspto-grants-1989_10