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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354839생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PiperazineHCID 4837—
반응물Sodium HydroxideHCID 14798—
반응물Sodium AcetateHCID 517045—
반응물2,3-Dihydro-1,4-benzodioxin-2-carbonyl chlorideHCID 2735447—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물1-(1,4-Benzodioxan-2-ylcarbonyl)piperazine hydrochlorideHCID 282243412.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04377581
출처 데이터셋uspto-grants-1983_03
ORD IDord-ad716962594649ddb4f9fab4437c3eb8
출처 메모uspto-grants-1983_03