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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1198435Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/1198435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
EduktSodium borohydrideHCID 4311764—
Edukt2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 13690761—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 1898441691,2%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05281592
Quelldatensatzuspto-grants-1994_01
ORD IDord-6f2afebbac264ddeb38dfa8207da9a4d
Quellennotizuspto-grants-1994_01