HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → alpha-(N-chloroacetyl-2-methyl-6-ethylphenylamino)acetaldehyde oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | alpha-(N-chloroacetyl-2-methyl-6-ethylphenylamino)acetaldehyde | HCID 20543832 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | alpha-(N-chloroacetyl-2-methyl-6-ethylphenylamino)acetaldehyde oxime | HCID 86736696 | 51.2% |
Reaction Steps
A solution of 5 g (0.2 mol) alpha-(N-chloroacetyl-2-methyl-6-ethylphenylamino)acetaldehyde, 3.3 g (0.04 mol) hydroxylamine hydrochloride and 3.4 g (0.04 mol) sodium bicarbonate in 50 ml ethanol was heated at 40° C. for 40 minutes. The reaction mixture was filtered, evaporated under reduced pressure, diluted with ethyl ether, filtered again and evaporated under reduced pressure to give 5.5 g of a yellow oil which crystallized to a solid on standing. The crude solid was recrystallized from ethyl ether/hexane to give 3.2 g of the product as a white solid, m.p. 113°-115° C. The product is tabulated in Table I as Compound No. 11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174210 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-cc90996c659640f8aa5a3289d48beb02 |
| Source note | uspto-grants-1979_11 |