HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → N-[(2,4-dichloro-1,3-thiazol-5-yl)methylidene]hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,4-Dichloro-1,3-thiazole-5-carboxaldehyde | HCID 1488672 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[(2,4-dichloro-1,3-thiazol-5-yl)methylidene]hydroxylamine | HCID 2778786 | 99% |
Reaction Steps
First 153 g (2.2 mol) of hydroxylamine hydrochloride in portions, then a solution of 364 g (2 mol) of 2,4-dichloro-5-thiazolecarboxaldehyde (II) in 1 liter of ethanol are added to a solution of 185 g (2.2 mol) of sodium bicarbonate in 5 liters of water at room temperature, with stirring. A voluminous, colourless precipitate separates out after 1 to 2 minutes. After stirring for 1 hour, the solid is filtered off with suction, washed with water and dried. 390 g (=99% of theory) of 2,4-dichloro-5-thiazolecarboxaldehyde oxime (IV) of melting point about 160° C. are obtained. It can be dehydrated to give the nitrile without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04555577 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-850e7a4834c34d218b58c255fcd44d36 |
| Source note | uspto-grants-1985_11 |