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HRID 354839作成日:2026年10月24日

Hydrochloric Acid → 1-(1,4-Benzodioxan-2-ylcarbonyl)piperazine hydrochloride

https://huagongshe.com/ja/reaction/354839

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PiperazineHCID 4837—
反応物Sodium HydroxideHCID 14798—
反応物Sodium AcetateHCID 517045—
反応物2,3-Dihydro-1,4-benzodioxin-2-carbonyl chlorideHCID 2735447—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物1-(1,4-Benzodioxan-2-ylcarbonyl)piperazine hydrochlorideHCID 282243412.3%

反応手順

A suspension of piperazine (11.88 g.) and sodium acetate (20.30 g.) in a mixture of water (70 ml.) and acetone (95 ml.) was stirred at 10°-15° C., then concentrated hydrochloric acid was added (about 35 ml.) until the pH of the solution reached 1.5. 1,4-Benzodioxan-2-carbonyl chloride (31.0 g.) and sodium hydroxide (5 N, about 45 ml.) were then added portionwise while maintaining the temperature at 10°-15° C., the sodium hydroxide maintaining the pH at 1.7-2.2. After the addition was complete, the pH was adjusted to 2.0 by the addition of sodium hydroxide, the suspension was stirred for a further 30 minutes. Water was then added until a homogeneous solution resulted, the acetone removed in vacuo, and the aqueous phase was basified to pH 8-9 with sodium hydroxide (5 N), re-extracted with chloroform (3×200 ml.) and the extracts washed with water, dried (MgSO4) and evaporated in vacuo. The oily residue was dissolved in ethyl acetate, treated with ethereal hydrogen chloride, evaporated in vacuo and the solid residue triturated with ether, followed by recrystallization from methanol to give N-(1,4-benzodioxan-2-carbonyl)-piperazine hydrochloride (4.85 g.), M.P. 265°-267° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04377581
出典データセットuspto-grants-1983_03
ORD IDord-ad716962594649ddb4f9fab4437c3eb8
出典メモuspto-grants-1983_03