HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 399415Erstellt: 23. Oktober 2026
Hydrochloric Acid → 2-chloro-4-[N'-(2-ethoxycarbonyl-1-acetylethylidene)hydrazino]benzoic acid
https://huagongshe.com/de/reaction/399415
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 3-Amino-4-chlorobenzoic acid | HCID 76092 | — |
| Edukt | Ethyl 3-acetyl-4-oxopentanoate | HCID 87820 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-chloro-4-[N'-(2-ethoxycarbonyl-1-acetylethylidene)hydrazino]benzoic acid | HCID 86753211 | — |
Reaktionsschritte
To a suspension of 1 gm. (5.8 mmoles) of 3 -amino-4-chlorobenzoic acid in 20 ml. of ethanol was added 5 ml. of water and 1 ml. of 12 N hydrochloric acid. The resultant solution was cooled in an ice bath and to the cooled solution was added in small portions 442 mg. (6.4 mmoles) of sodium nitrite in 3 ml. of water. The mixture was allowed to warm to room temperature and after 30 minutes was added to a suspension of 1.19 gm. (6.4 mmole) of ethyl 3-acetyl-4-oxopentanoate, 1.8 gm. of sodium acetate, 20 ml. of ethanol and 5 ml. of water. The reaction mixture turned dark orange. After stirring for one hour, the mixture was acidified with 3 N hydrochloric acid and the resultant solids collected by filtration. After drying the material, 2.53 g. was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05821243 |
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| Quelldatensatz | uspto-grants-1998_10 |
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| ORD ID | ord-cfd35857535145c487ef71836db4a77d |
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| Quellennotiz | uspto-grants-1998_10 |
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