참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Piperazine | HCID 4837 | — |
| 반응물 | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | 1-(4-Nitrophenyl)piperazine | HCID 80447 | 70% |
반응 단계
A solution of 1-chloro-4-nitrobenzene (15 g, 94.5 mmol) in 1-butanol (75 mL) was added over 20-30 minutes to a refluxing solution of anhydrous piperazine (24.4 g, 284 mmol) in 1-butanol (75 mL) and the mixture maintained at reflux overnight. The solvent was removed under reduced pressure to afford a solid, to which was added 2N hydrochloric acid (400 mL). The aqueous layer was washed twice with ethyl acetate, cooled to below 10° C. and basified with a cold solution of 40% sodium hydroxide to pH 10, keeping temperature below 20° C. The mixture was extracted with ethyl acetate (4×200 mL) then the combined organic layers were washed with brine and dried over sodium sulfate. Filtration and concentration under reduced pressure afforded 1-(4-nitro-phenyl)-piperazine (13.7 g, 70%) as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524705B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-d7d2de766a46414ba628539baf8c1656 |
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| 출처 메모 | uspto-grants-2013_09 |
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