HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402099Erstellt: 25. Oktober 2026
Hydrogen Bromide → 5-Bromo-2-methylbenzothiazole
https://huagongshe.com/reaction/402099
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | 2-Methylbenzothiazol-5-ylamine dihydrochloride | HCID 16218943 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Katalysator | copper(I) bromide | HCID 24593 | — |
| Produkt | 5-Bromo-2-methylbenzothiazole | HCID 3017457 | — |
Reaktionsschritte
Sodium nitrite (0.9 g, 13 mmol) was added portionwise to a suspension of 2-methyl-5-aminobenzothiazole dihydrochloride (2.0 g, 8 mmol) in hydrobromic acid (24 ml) at 0° C. The resulting mixture was added dropwise to a solution of copper(I) bromide (4.0 g, 14 mmol) in hydrobromic acid (50 ml) at 0° C. After stirring at 0° C. for 2 hours, water was added. The reaction mixture was basified to pH 9 using aqueous ammonium hydroxide and was extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate to give 2-methyl-5-bromobenzothiazole (1.0 g, 52%, 82% AUC GC) after chromatography (9:1 heptane/ethyl acetate): 1H NMR (300 MHz, DMSO-d6) δ 8.12 (d, J=1.8 Hz, 8.02 (dd, 1H) J=8.4, 1.5 Hz, 1H), 7.56 (dd, J=8.7, 2.1 Hz, 1H), 2.81 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08741901B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-3746329ea75a4ae38673c27b0a05bc27 |
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| Quellennotiz | uspto-grants-2014_06 |
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