HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloral → Acetamide, 2-(hydroxyimino)-N-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloral | HCID 6407 | — |
| Reactant | 3,5-Dichloroaniline | HCID 12281 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acetamide, 2-(hydroxyimino)-N-phenyl- | HCID 6861488 | — |
Reaction Steps
To a solution of trichloroacetaldehyde monohydate (13.25 g, 1.3 eq) in H2O (150 mL) was successively added sodium sulfate (17.55 g, 4.0 eq), a hot solution (ca. 80° C.) of 3,5-dichloroaniline (10.0 g, 61.5 mmol) in H2O (50 mL) and 37% HCl (6.1 mL), and a solution of hydroxylamine hydrochloride (16.3 g, 3.8 eq) in H2O (75 mL) with rapid stirring. Once the addition was completed the reaction mixture was heated at reflux for 2 minutes and then allowed to cool to room temperature. The resulting light brown precipitate was filtered, washed with H2O (200 mL) and then dried to yield the crude isonitrosoacetanilide (20.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576656B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-62e3b4db55134910b92355b50077dc92 |
| Source note | uspto-grants-2003_06 |