HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydroxylamine → 2,3-Difluoro-6-(trifluoromethyl)benzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydroxylamine | HCID 787 | — |
| Edukt | 2,3-Difluoro-6-(trifluoromethyl)benzonitrile | HCID 10104456 | — |
| Katalysator | Ferrous Chloride | HCID 24458 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2,3-Difluoro-6-(trifluoromethyl)benzamide | HCID 22010119 | — |
| Produkt | 2,3-Difluoro-N-hydroxy-6-(trifluoromethyl)benzimidamide | HCID 54418213 | — |
Reaktionsschritte
In a colorless, transparent glass reaction vessel was placed a mixed solvent of 150 ml of methanol-distilled water (volume ratio 1:2) into which were dissolved beforehand 9.91 g (150 mmol) of 50% hydroxylamine aqueous solution and on purpose 86 μg (0.00068 mmol) of iron(II) chloride. Into the mixed solvent was added 10.36 g (50.0 mmol) of 2,3-difluoro-6-trifluoromethylbenzonitrile (I″). The reaction temperature stood at 60° C. for 6 hours and was returned to room temperature. In HPLC analysis of the reaction solution, it was shown that (I″) disappeared, 2,3-difluoro-6-trifluoromethylbenzamidoxime (II′) was mainly produced (yield 62.4%) and 2,3-difluoro-6-trifluoromethylbenzamide (III′) was noticeably produced as a byproduct (yield 22.8%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06211232B1 |
| Quelldatensatz | uspto-grants-2001_04 |
| ORD ID | ord-5267a7ccf8004844acdb99cd63e39033 |
| Quellennotiz | uspto-grants-2001_04 |