HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234165Erstellt: 26. Oktober 2026
Phenethyl bromide → 3-(2-phenylethyl)-1,3-benzothiazol-2(3H)-one
https://huagongshe.com/reaction/234165
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenethyl bromide | HCID 7666 | — |
| Edukt | Benzothiazolone | HCID 13625 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-(2-phenylethyl)-1,3-benzothiazol-2(3H)-one | HCID 1093146 | 80% |
Reaktionsschritte
(1aB) Benzothiazolin-2-one (5.15 g, 34.1 mmol) was dissolved in dimethylformamide (100 ml) and to the solution was added 60% sodium hydride (1.36 g, 34.1 mmol) which was stirred at room temperature until generation of hydrogen gas stopped. Then β-phenylethylbromide (4.89 ml, 35.8 mmol) was added to the solution which was stirred at room temperature for 17 hours. To the reaction solution was added a saturated aqueous solution of ammonium chloride, followed by extraction with ethyl acetate. The organic layer was washed in turn with a saturated sodium bicarbonate solution and saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The crude product thus obtained was purified by subjecting it to silica gel column chromatography to give 6.49 g of 3-phenethylbenzothiazoline-2-one as a white amorphous powder form n-hexane/ethyl (4:1)-eluted fraction (yield: 80%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05594144 |
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| Quelldatensatz | uspto-grants-1997_01 |
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| ORD ID | ord-456553774f75411b9d86aa476cb84047 |
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| Quellennotiz | uspto-grants-1997_01 |
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