Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Edukt | Methyl 3-bromo-5-iodobenzoate | HCID 21942573 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (3-Bromo-5-iodophenyl)methanol | HCID 15467379 | 96,7% |
Reaktionsschritte
To methyl 5-bromo-3-iodobenzoate (Step A above) (5.01 g, 0.015 mole) in anhydrous methylene chloride (100 mL) at -78° C., was added dropwise minutes, diisobutylaluminum hydride (5.50 mL, 0.03 mole). The mixture was stirred for 1 hour then allowed to warm to 0° C. The reaction solution was poured into 600 mL, chilled 3N HCl and extracted 3× with methylene chloride (150 mL). The organic layers were combined, dried over MgSO4 and concentrated under vacuum to yield 5-bromo-3-iodobenzyl alcohol (4.54 g) as a white solid. MP=110-112° C. MS and NMR were consistent with the desired structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06028223 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-7a3136ee0bb84c16864a250cede4929f |
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| Quellennotiz | uspto-grants-2000_02 |
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