HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 5-(6-bromonaphthalen-2-yl)-N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenylbenzene-1,3-Diamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,6-Dibromonaphthalene | HCID 640591 | — |
| Edukt | N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diamine | HCID 68193967 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-(6-bromonaphthalen-2-yl)-N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenylbenzene-1,3-Diamine | HCID 68193747 | — |
Reaktionsschritte
13.42 g of a product (yield: 66%) was obtained in the same manner as described in the synthesis method of intermediate 2-3 except that N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diamine (17.76 g, 30 mmol), 2,6-dibromonaphthalene (9.44 g, 33 mmol), Pd(PPh3)4 (1.04 g, 0.9 mmol), K2CO3 (12.44 g, 90 mmol), THF (90 mL), and water (45 mL) were used.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09102616B2 |
| Quelldatensatz | uspto-grants-2015_08 |
| ORD ID | ord-17559f20e43e4b8f8c2a43fb252975b4 |
| Quellennotiz | uspto-grants-2015_08 |