HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742278Generated: October 31, 2026
Hydrochloric Acid → 6-(Benzenesulfonyl)-2,3-dihydropyridazin-3-one
https://huagongshe.com/reaction/1742278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Benzenesulfinic acid, sodium salt, dihydrate | HCID 23681562 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(Benzenesulfonyl)-2,3-dihydropyridazin-3-one | HCID 11701437 | 69% |
Reaction Steps
A mixture of 3,6-dichloropyridazine (50 g), sodium benzenesulfinate dihydrate (100 g), benzyltrimethylammonium chloride (62.3 g), and 1,4-dioxane (335 ml) was stirred for 3 hours at 100° C. After being cooled to room temperature, aqueous solution of sodium hydroxide (510 ml) was added to the mixture, and the mixture was stirred for 0.5 hour at 100° C. The reaction mixture was cooled in a water bath and acidified with 36% hydrochloric acid (35 ml). The precipitate formed was collected, washed well with water, and dried to give 6-phenylsulfonyl-3-oxo-2,3-dihydropyridazine (54.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05338743 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-bd7e5a0f947a452c980a4552d273cfdd |
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| Source note | uspto-grants-1994_08 |
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