Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Triethylsilane | HCID 12052 | — |
| Edukt | 1-(7-Bromo-benzo[1,3]dioxol-5-yl)-2-methyl-propan-1-ol | HCID 18445394 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Bromo-6-isobutyl-benzo[1,3]dioxole | HCID 18445415 | 52% |
Reaktionsschritte
To a cold solution (0° C.) of 1-(7-bromo-benzo[1,3]dioxol-5-yl)-2-methyl-propan-1-ol (498 mg, 1.82 mmol) in dry dichloromethane (10 mL) was added triethylsilane (0.6 mL, 3.65 mmol). After 15 minutes, trifluoroacetic acid was added to the reaction and the mixture stirred at 0° C. for 45 minutes. Water was poured into the reaction mixture and the layers separated. The organic layer was further washed with water, aqueous NaHCO3 and brine, dried (MgSO4), filtered and evaporated. The residue was purified on silica gel (5% ethyl acetate in hexane) to give 242 mg of 4-bromo-6-isobutyl-benzo[1,3]dioxole (52%). 1H NMR (300 MHz; CDCl3): δ 0.90 (d, J=6.3 Hz, 6H), 1.81 (m, 1H), 2.39 (d, J=7.5 Hz, 2H), 6.01 (s, 2H), 6.58 (s, 1H), 6.76 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07196108B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-6fcf7cb8bdb94600a5a6b80f990952fd |
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| Quellennotiz | uspto-grants-2007_03 |
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