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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1439862Erstellt: 25. Oktober 2026

Potassium Hydroxide → (R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/1439862

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt(R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalene-sulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazineHCID 54249707—
LösungsmittelWater ethanolHCID 19096565—
Produkt(R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 2284749458,7%

Reaktionsschritte

(R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalenesulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazine (9.40 g, 0.017 mole) is suspended in ethanol-water (10:1, 188 ml), and thereto is added 86 % potassium hydroxide (11.2 g, 0.172 mole), and the mixture is refluxed for 30 minutes. The reaction mixture is poured into ice water and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed with water and saline, dried over sodium sulfate and distilled to remove the solvent. The residue is purified by silica gel column chromatography (CHC13) and thereafter recrystallized from ethyl acetate-hexane twice to give (R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (2.61 g, 58%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05496815
Quelldatensatzuspto-grants-1996_03
ORD IDord-dd8f4106bf8145ac974452eea81d74c7
Quellennotizuspto-grants-1996_03