HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → HCID 68138846, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 68140652 | HCID 68140652 | — |
| Reactant | HCID 86733435 | HCID 86733435 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68138846 | HCID 68138846 | — |
Reaction Steps
In an analogous manner, from 0.6 g. 3-(5-nitro-2-furyl)-6-(ethoxy-methylene)-amino-s-triazolo[4,3-b]pyridazine in 12 ml. anhydrous dioxan and an ethanolic solution of hydroxylamine (prepared from 0.6 g. hydroxylamine hydrochloride in 15 ml. absolute ethanol by adding 0.14 g. sodium, dissolved in 5 ml. absolute ethanol, and filtering off with suction the precipitated sodium chloride) at 50° - 60°C., there was obtained, after a reaction period of 15 minutes and cooling of the reaction mixture, 0.55 g. 3-(5-nitro-2-furyl)-6-(hydroxylaminomethylene)-amino-s-triazolo[4,3-b]pyridazine, which melted, with foaming, at 251° - 253°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03957766 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-64304a03fc654fddb4b53e7c875064c7 |
| Source note | uspto-grants-1976_05 |