Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1886667생성일: 2026년 10월 25일
1-Benzylpiperazine → 1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazine
https://huagongshe.com/reaction/1886667
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Benzylpiperazine | HCID 75994 | — |
| 반응물 | 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride | HCID 15053367 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazine | HCID 15053405 | 108.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05151418 |
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| 출처 데이터셋 | uspto-grants-1992_09 |
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| ORD ID | ord-e85d4c3b1910426fbbe4be17e1b79c9a |
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| 출처 메모 | uspto-grants-1992_09 |
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