HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Iodophenol | HCID 12272 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Magnesium Chloride | HCID 5360315 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2-Hydroxy-4-iodobenzaldehyde | HCID 18351513 | 160,1% |
Reaktionsschritte
To a solution of 3-iodophenol (3.00 g, 13.6 mmol) in acetonitrile (50 mL) was added magnesium chloride (3.89 g, 40.9 mmol), triethylamine (7.6 mL, 55 mmol), and paraformaldehyde (1.64 g, 55 mmol). The reaction mixture was refluxed overnight, then neutralized with saturated aqueous ammonium chloride. The resultant red precipitate was removed by filtration, and the filtrate was extracted with ethyl acetate. The precipitate was dissolved in methanol and added to the combined organic extracts, which were then dried over magnesium sulfate. The solvent was removed under reduced pressure to provide an orange solid (5.4 g) as the crude product. This material was used in the subsequent step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07420066B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-02721cc0f01345be9e12390ff0c5239e |
| Quellennotiz | uspto-grants-2008_09 |