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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974631생성일: 2026년 10월 25일

1-Benzylpiperazine → 1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazine

https://huagongshe.com/reaction/974631

반응식

참여 물질

역할이름HCID투입량
반응물1-BenzylpiperazineHCID 75994—
반응물3-(4-Fluorophenoxy)-1-azetidinecarbonyl chlorideHCID 15053367—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazineHCID 15053405108.3%

반응 단계

A stirred solution of 6.9 g (0.03 mole) of 3-(4-fluorophenoxy)-1-azetidinecarbonyl chloride in 60 ml of methylene chloride was treated with 10.8 g (0.06 mole) of 1-benzylpiperazine, added dropwise. After stirring for 18 hr, the reaction mixture was diluted with 200 ml of water and stirred for an additional 1 hr. The methylene chloride portion was separated and the aqueous portion was extracted with 2×25 ml of methylene chloride. The methylene chloride portions were combined, dried and concentrated in vacuo, yielding 12 g of oil residue. This oil solidified when triturated with ligroin and was recrystallized from benzene/ligroin to yield 10.1 (91%) of tan crystals. A 500 mg portion was recrystallized from benzene/ligroin to yield 250 mg of fine white crystals, m.p. 109°-111° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05068231
출처 데이터셋uspto-grants-1991_11
ORD IDord-5f5af5613f124eeea030e37d7a602d3c
출처 메모uspto-grants-1991_11