Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Hexamethylenetetramine | HCID 4101 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | 4-Bromophenol | HCID 7808 | — |
| Produkt | 5-Bromo-2-hydroxybenzene-1,3-dicarbaldehyde | HCID 5260206 | 60% |
Reaktionsschritte
Hexamethylenetetramine (73.84 g, 526 mmol) was added to TFA (240 mL) with stirring. 4-Bromophenol (22.74 g, 131 mmol) was added in one portion and the solution heated in an oilbath to 120° C. and stirred under argon for 48 h. The reaction mixture was then cooled to ambient temperature. Water (160 mL) and 50% aqueous H2SO4 (80 mL) were added and the solution stirred for an additional 2 h. The reaction mixture was poured into water (1600 mL) and the resulting precipitate collected on a Büchner funnel. The precipitate was dissolved in ethyl acetate (EtOAc) and the solution was dried over MgSO4. The solution was filtered and the solvent removed on a rotary evaporator. Purification by column chromatography on silica gel (400 g) using a gradient of 15-40% ethyl acetate in hexanes resulted in a isolation of the product as a yellow solid (18.0 g, 60%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07563890B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-3ccd582506cc438a9f5ab5bb44403382 |
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| Quellennotiz | uspto-grants-2009_07 |
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