HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Isopropanol → 1-Chloro-3-(4-fluorophenyl)hex-5-en-3-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Binol | HCID 11762 | — |
| Edukt | 2-Chloro-4'-fluoropropiophenone | HCID 67672 | — |
| Edukt | Tetrallylstannane | HCID 81878 | — |
| Katalysator | Titanium isopropoxide | HCID 11026 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-Chloro-3-(4-fluorophenyl)hex-5-en-3-ol | HCID 53472938 | — |
Reaktionsschritte
To a solution of 1,1′-bi-2-naphthol (0.2280 g, 0.80 mmol, 0.26 equiv), CH2Cl2 (5 mL) and titanium(IV) isopropoxide (0.2243 g, 0.79 mmol, 0.26 equiv) were added 2-propanol (3.1620 g, 52.6 mmol, 17 equiv), tetraallylstannane (1.2538 g, 4.43 mmol, 1.43 equiv), and 3-chloro-1-(4-fluorophenyl)propan-1-one (0.5760 g, 3.09 mmol, 1.0 equiv) successively. The reaction mixture was stirred at rt under nitrogen for 22 h. The reaction was quenched with satd aq NH4Cl and extracted with EtOAc. The organic layer was dried over Na2SO4. After the solvents were evaporated, the residue was purified by chromatography on silica gel eluted with hexanes/ethyl acetate to afford 1-chloro-3-(4-fluorophenyl)hex-5-en-3-ol as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08487094B2 |
| Quelldatensatz | uspto-grants-2013_07 |
| ORD ID | ord-f38ad47adc164f30938f3185cfebd733 |
| Quellennotiz | uspto-grants-2013_07 |