HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydroxylamine → 2,3-Difluoro-6-(trifluoromethyl)benzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydroxylamine | HCID 787 | — |
| Edukt | 1,10-Phenanthroline | HCID 1318 | — |
| Edukt | 2,3-Difluoro-6-(trifluoromethyl)benzonitrile | HCID 10104456 | — |
| Lösungsmittel | Methanol--water (1/1) | HCID 22242641 | — |
| Produkt | 2,3-Difluoro-6-(trifluoromethyl)benzamide | HCID 22010119 | — |
| Produkt | 2,3-Difluoro-N-hydroxy-6-(trifluoromethyl)benzimidamide | HCID 54418213 | — |
Reaktionsschritte
Into an SUS reaction vessel was placed a mixed solvent of 1.5 L of methanol-water (volume ratio 1:2, tap water was used as water) into which 99.09 g (1.50 mol) of 50% hydroxylamine aqueous solution and 198 mg (1.00 mmol) of o-phenanthroline were dissolved beforehand. Into the mixed solvent was added 103.56 g (500 mmol) of 2,3-difluoro-6-trifluoromethylbenzonitrile (I″). The reaction temprature stood at 60° C. for 7 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 78.9%) and 2,3-difluoro6-trifluoromethylbenzamide (III′) was produced as a byproduct (yield 9.0%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06211232B1 |
| Quelldatensatz | uspto-grants-2001_04 |
| ORD ID | ord-b1d9c881048140e0a746460025686ef2 |
| Quellennotiz | uspto-grants-2001_04 |