HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → 4-amino-2,6-dichloro-N'-hydroxy-alpha,alpha-dimethylbenzeneethanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 2-(4-Amino-2,6-dichloro-phenyl)-2-methyl-propionitrile | HCID 11241669 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-amino-2,6-dichloro-N'-hydroxy-alpha,alpha-dimethylbenzeneethanimidamide | HCID 54422643 | 26% |
Reaction Steps
NaOCH3 30% (0.592 mole) was added to a solution of hydroxylamine hydrochloride (0.1085 mole) in CH3OH (200 ml), stirred at RT. The mixture was stirred for 10 minutes. Intermediate (3) (0.0542 mole) was added portionwise and the resulting reaction mixture was stirred and refluxed overnight. The solvent was evaporated. The residue was partitioned between CH2Cl2 and water. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was stirred in DIPE, filtered off, washed with DIPE, and dried, yielding 3.7 g (26%) of 4-amino-2,6-dichloro-N′-hydroxy-α,α-dimethylbenzeneethanimidamide (intermediate 17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911444B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-3dec2af875394d3ea42fa5292f0f9541 |
| Source note | uspto-grants-2005_06 |