戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5823作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/5823

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物Sodium borohydrideHCID 4311764—
反応物2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 13690761—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 1898441691.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246929
出典データセットuspto-grants-1993_09
ORD IDord-ac2c06d7cbfb4525b6d01a68903c4d4b
出典メモuspto-grants-1993_09