HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Acid → 7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene | HCID 10586063 | — |
| Katalysator | chromium (VI) trioxide | HCID 10219390 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10753357 | — |
Reaktionsschritte
To a cold mixture (0° C.) of 209 g (200 mmol) of chromium trioxide, 100 ml (1.06 mol) of acetic anhydride and 200 ml (3.5 mol) of acetic acid was added a solution of 10 g (41.8 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound F) in 125 ml of benzene. The reaction mixture was stirred for 1 hour, quenched with ice cold water and extracted with Et2O (3×100 ml). The organic layer was dried over MgSO4, concentrated in vacuo, and purified by column chromatography (silica, 10% EtOAc-hexane) to give the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05723666 |
| Quelldatensatz | uspto-grants-1998_03 |
| ORD ID | ord-cfa73652b7a144b88fc260b76438c1a1 |
| Quellennotiz | uspto-grants-1998_03 |