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HRID 1439862作成日:2026年10月26日

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

https://huagongshe.com/reaction/1439862

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物(R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalene-sulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazineHCID 54249707—
溶媒Water ethanolHCID 19096565—
生成物(R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 2284749458.7%

反応手順

(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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05496815
出典データセットuspto-grants-1996_03
ORD IDord-dd8f4106bf8145ac974452eea81d74c7
出典メモuspto-grants-1996_03