Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromohexane | HCID 8101 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-Bromo-6-(hexyloxy)naphthalene | HCID 4535583 | 81% |
Reaktionsschritte
To a stirred solution of 4.46 g (20.0 mmol) of 6-bromo-2-naphthalenol (obtained from Aldrich Chemical Company (#B7,340-6) and used without purification), in 20 mL of DMF at room temperature under argon was added 480 mg (20 mmol) of 95% sodium hydride over the course of 15 min. The resulting light yellow solution was stirred 30 min and 3.5 mL (22 mmol) of 1-bromohexane was added. The reaction was heated to 50° C. and stirred for 60 min. The reaction was quenched with ice water, the resultings solids filtered, washed with water and dried in vacuo at 60° C. Purification of the residue by chromatography on silica gel (5×20 cm column, hexanes as elutant) gave 5.00 g, 81% yield, of title compound as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05470845 |
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| Quelldatensatz | uspto-grants-1995_11 |
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| ORD ID | ord-ea0be3f4da6145b1a42c817acc44334a |
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| Quellennotiz | uspto-grants-1995_11 |
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