HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanol → 2,6-Dichloro-3-nitrobenzylideneaminooxyacetic Acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | Aminooxyacetic acid hemihydrochloride | HCID 2723609 | — |
| Edukt | 2,6-Dichloro-3-nitrobenzaldehyde | HCID 2794912 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2,6-Dichloro-3-nitrobenzylideneaminooxyacetic Acid | HCID 131713326 | — |
Reaktionsschritte
A warm solution of 2,6-dichloro-3-nitrobenzaldehyde, 1.8 gm. in 20 ml. of ethanol was stirred into a solution of 0.9 gm. (0.008 equivs.) of carboxymethoxylamine hemihydrochloride and 0.45 gm. of sodium acetate, anhyd., in 20 ml. of water at room temperature. The mixture was heated on the steam bath for one-half hour, and was then evaporated to dryness at room temperature. The residue was triturated with cold water, filtered, washed with cold water and dried in air to obtain 2.1 gm. (87.4%) of crude material melting at 76°-84° C. This was purified from aqueous-methanol to obtain 1.9 gm. of pale cream-colored product melting at 82°-85° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04423241 |
| Quelldatensatz | uspto-grants-1983_12 |
| ORD ID | ord-53d2f437ebe943f9bff6bf863ea181a4 |
| Quellennotiz | uspto-grants-1983_12 |