HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Boron trifluoride → (4,5-Difluoro-7-nitro-benzofuran-6-yl)-(2-fluoro-4-iodo-phenyl)-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Boron trifluoride | HCID 6356 | — |
| Edukt | 3-(2,2-Diethoxyethoxy)-5,6-difluoro-N-(2-fluoro-4-iodophenyl)-2-nitroaniline | HCID 86671488 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (4,5-Difluoro-7-nitro-benzofuran-6-yl)-(2-fluoro-4-iodo-phenyl)-amine | HCID 67235416 | 69,5% |
Reaktionsschritte
For scale up, a solution of 3-(2,2-diethoxyethoxy)-5,6-difluoro-N-(2-fluoro-4-iodophenyl)-2-nitroaniline (75 g) in 300 mL of DCM was added quickly into a solution of BF3.ET2O in 100 mL of DCM at 28-32° C. with further stirring for 15 minutes. After about 2 hours, analysis showed complete conversion. The solution was then quenched by 1N NaOH (dropwise) at a temperature below 30° C. to pH 10 before separating. DCM was then washed with water twice to a pH of about 7 and concentrated to dryness. 210 mL of MBTE was then added. The suspension was stirred for 30 minutes, filtered and dried to give 43 g of an orange solid. 1H NMR (CDCl3, 400 MHz): δ 8.80 (bs, 1H), 7.75 (d, 1H), 7.48 (dd, 1H), 7.41 (d; 1H); 6.97 (d, 1H), 6.75-6.80 (m, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08470878B2 |
| Quelldatensatz | uspto-grants-2013_06 |
| ORD ID | ord-fc3a9e148aff401695f59c03e0aef737 |
| Quellennotiz | uspto-grants-2013_06 |