HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 327757Erstellt: 24. Oktober 2026
Hydrochloric Acid → 3-(Benzothiazol-2-yl)-4-Phenyl-2-(5H) Furanone
https://huagongshe.com/de/reaction/327757
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Ethanone, 2-(acetyloxy)-1-phenyl- | HCID 222851 | — |
| Edukt | alpha-(Benzothiazol-2-yl)-acetate | HCID 7128533 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 3-(Benzothiazol-2-yl)-4-Phenyl-2-(5H) Furanone | HCID 54181341 | — |
Reaktionsschritte
A solution of 2-acetoxyacetophenone (from Example 1) (8.9 g, 0.05M) and α-(benzothiazol-2-yl)-acetate (from Example 3) dissolved in methanol (40 mL) by stirring at room temperature was treated at room temperature with a solution prepared by dissolving sodium hydroxide pellets (2.5 g) in methanol (30 mL) by stirring. A slight exothermic reaction was observed. After being stirred at about room temperature for about 1.0 hour, the reaction mixture was acidified to a pH of about 4 by the dropwise addition of concentrated HCl. The product which was a dark brown colored semi-crystalline mass was washed by decantation and dried in air (yield--12.0 g (81.9% of the theoretical yield). Mass spectrometry indicated that the product largely consisted of the following desired compound: ##STR16##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05274072 |
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| Quelldatensatz | uspto-grants-1993_12 |
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| ORD ID | ord-6a524c00b0354527b91f0643f335c8bc |
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| Quellennotiz | uspto-grants-1993_12 |
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