HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1266950Erstellt: 25. Oktober 2026
2-Bromoethanol → Benzothiazolium, 3-(2-hydroxyethyl)-6-methoxy-2-methyl-, bromide (1:1)
https://huagongshe.com/reaction/1266950
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Bromoethanol | HCID 10898 | — |
| Edukt | 6-Methoxy-2-methylbenzothiazole | HCID 76254 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Benzothiazolium, 3-(2-hydroxyethyl)-6-methoxy-2-methyl-, bromide (1:1) | HCID 114275 | 30% |
Reaktionsschritte
A solution of 6-methoxy-2-methylbenzothiazole (1.82 g) and 2-bromoethanol (8.8 g) was stirred and heated in an oil bath at 120° C. for 74 hours. After cooling the reaction mixture to room temperature, adding ethyl acetate (25 ml) and stirring for 1 hour, the solid was filtered and collected. The solid was then dissolved in methanol (50 ml) and charcoal (0.5 g) was added. The charcoal was removed by passing through a pad of Celite®. The solution was then concentrated to a small volume and triturated with ethyl acetate (100 ml). The solid was collected, washed with ethyl acetate (2×30 ml) and dried in an oven under high vacuum at 50° C. overnight to obtain 0.9 g (30%) of 4c.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06551831B2 |
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| Quelldatensatz | uspto-grants-2003_04 |
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| ORD ID | ord-b2c931b31a6644eeab10b83fba1e1aee |
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| Quellennotiz | uspto-grants-2003_04 |
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