HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5823Erstellt: 24. Oktober 2026
Hydrochloric Acid → 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
https://huagongshe.com/de/reaction/5823
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-one | HCID 13690761 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine | HCID 18984416 | 91,2% |
Reaktionsschritte
To a mixture of 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (4.0 g), sodium borohydride (2.91 g) and tetrahydrofuran (100 ml) is added dropwise with stirring boron trifluoride etherate complex (12. 5 ml) at room temperature, and the mixture is refluxed for 1.5 hour. After cooling, to the mixture is added dropwise 10% hydrochloric acid (35 ml), and the mixture is further refluxed for one hour. The reaction mixture is poured into ice water and made alkaline with potassium carbonate and extracted with ethyl acetate. The ethyl acetate layer is washed, dried and distilled to remove the solvent. The residue is recrystallized from isopropyl ether to give 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (3.45 g, yield 91%) as crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05246929 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-ac2c06d7cbfb4525b6d01a68903c4d4b |
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| Quellennotiz | uspto-grants-1993_09 |
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