HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chlorosuccinimide → N-Hydroxy-2-methylbenzene-1-carboximidoyl chloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | 2-Methyl-benzaldoxime | HCID 102401 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-Hydroxy-2-methylbenzene-1-carboximidoyl chloride | HCID 71403975 | 74% |
Reaktionsschritte
N-Chlorosuccinimide (2.22 g, 16.6 mmol, 1.0 equiv) was added to a stirred solution of 2-methyl-benzaldehyde oxime (2.25 g, 16.6 mmol, 1.0 equiv) in N,N-dimethylformamide (30 mL) at ambient temperature. Stirring was continued for 2 hours and the reaction quenched (ice-water). The resultant mixture was extracted with ethyl acetate. The combined organic extracts were washed sequentially with water (6×) and saturated aqueous sodium chloride solution (2×). The organic was then dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to give 2.07 g (74%) of N-hydroxy-2-methylbenzenecarboximidoyl chloride as a green oil. 1H NMR (300 MHz, CDCl3) δ: 8.14 (s, 1H), 7.48-7.44 (m, 1H), 7.37-7.20 (m, 3H), 2.43 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08637526B2 |
| Quelldatensatz | uspto-grants-2014_01 |
| ORD ID | ord-360efc0fbb804bd8b06eabe18bbdf9b6 |
| Quellennotiz | uspto-grants-2014_01 |