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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379393Generated: October 27, 2026

Ammonia → HCID 178515449, compound

https://huagongshe.com/reaction/2379393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4'-Chlorophenyl)-4-hydroxy-6-bromopyridazine 3-(4'-Chlorophenyl)-4,6-dibromopyridazineHCID 178477992—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178515449HCID 178515449—

Reaction Steps

3-(4'-Chlorophenyl)-4-hydroxy-6-bromopyridazine 3-(4'-Chlorophenyl)-4,6-dibromopyridazine (52.2 g, 0.1498 mol) was dissolved in hot dioxane (300 ml) and a solution of 12 g (0.3 mol) of sodium hydroxide solution in 50 ml of water was added dropwise in the course of 10 minutes while the mixture was refluxed gently. The mixture was maintained under reflux for a further 4.5 hours, the dioxane was evaporated in vacuo, and the solid residue was dissolved in 1 l of hot water (95° C.). A small amount of solid product (tarry) was filtered under hot conditions with the aid of animal charcoal, and the hydrolysis product was precipitated using hydrochloric acid. The product which had been isolated (solid) by filtering off with suction was, while still moist, suspended in 1 l of water, after which process the pH of the suspension, at 65° C., was brought to 9-10 using ammonia. Most of the product dissolved, and the insoluble components were isolated and again treated with ammonia. The combined filtrates were then acidified using hydrochloric acid, and the 3-(4'-chlorophenyl)-4-hydroxy-6-bromopyridazine which was obtained was isolated, washed with water and dried to constant weight. 27.5 g, 0.09631 mol, 64.3% of theory, m.p.=262°-264° C. was thereby obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362708
Source datasetuspto-grants-1994_11
ORD IDord-8ad715da7dd5433dadad37174a178f2e
Source noteuspto-grants-1994_11