HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391015Erstellt: 23. Oktober 2026
Acetamidine monohydrochloride → 5-Bromo-2-methylpyrimidine-4-carboxylic acid
https://huagongshe.com/de/reaction/391015
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetamidine monohydrochloride | HCID 67170 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Mucobromic Acid | HCID 3033972 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-Bromo-2-methylpyrimidine-4-carboxylic acid | HCID 256210 | 25,4% |
Reaktionsschritte
To a solution of acetamidine hydrochloride (6.0 g) in ethanol (20 mL) was added sodium ethoxide (20 mL of a 21% solution in ethanol) and the reaction mixture was heated at 50° C. and mucobromic acid (6.82 g) in ethanol (10 mL) was added. After stirring at 50° C. for 1 h, a further portion of sodium ethoxide (10 mL of a 21% solution in ethanol) was added and the mixture was stirred at room temperature for 16 h. The mixture was then filtered and the filtrate reduced in vacuo. The residue was then treated with 2 M aqueous hydrochloric acid (30 mL) and stirred vigorously for 30 minutes. The resulting solid was filtered, washed with water and air dried to give 5-bromo-2-methyl-pyrimidine-4-carboxylic acid (1.46 g). This was then heated at 175° C. for 16 h. After cooling to room temperature the mixture was purified by Kugelrohr distillation to give 5-bromo-2-methyl-pyrimidine as a white solid (746 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08383620B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-9cbfc31e361648e0a7a4ffb10d1c6fd4 |
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| Quellennotiz | uspto-grants-2013_02 |
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