HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Thiophenol → 4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Thiophenol | HCID 7969 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10753357 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene | HCID 15896018 | — |
Reaktionsschritte
To a stirred solution of 4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one (Compound G, 1.48 g, 5.9 mmol), titanium tetrachloride (1.09 g, 5.7 mmol) and THF (10 mL) was added a mixture of thiophenol (660 mg, 6 mmol), triethylamine (1.16 g, 11.5 mmol) and THF (20 mL) via an addition funnel at ambient temperature. The mixture was stirred for 5 h, and water (10 mL) was added, extracted with ether (3×50 mL). The combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried (MgSO4) and the solvent distilled off at reduced pressure. After silicagel chromatography the title compound was obtained as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05723666 |
| Quelldatensatz | uspto-grants-1998_03 |
| ORD ID | ord-becf0ee7c3024fadba4ea32c31403111 |
| Quellennotiz | uspto-grants-1998_03 |