Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4318생성일: 2026년 10월 24일
Hydrochloric Acid → 1,3-Bis[4-(3-chlorobenzyl)-1-piperazinyl]propane dihydrochloride monohydrate
https://huagongshe.com/ko/reaction/4318
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1-Bromo-3-chloropropane | HCID 8006 | — |
| 반응물 | 1-(3-Chlorobenzyl)piperazine | HCID 764727 | — |
| 반응물 | Dichloromethane methanol ammonium hydroxide | HCID 21896990 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 1,3-Bis[4-(3-chlorobenzyl)-1-piperazinyl]propane dihydrochloride monohydrate | HCID 20152239 | 68% |
반응 단계
A mixture of 6.3 g of 1-(3-chlorobenzyl)piperazine, 2.4 g of 1-bromo-3-chloropropane, 50 ml of reagent ethanol and 3.0 g of triethylamine was refluxed for 4 hours. Water (70 ml) was added, and the mixture was concentrated under vacuum to about 70 ml. The resulting aqueous mixture was extracted with ether (3×150 ml), and the extract was concentrated under vacuum to give a reddish-yellow oil. Chromatography of this oil on a silica column, the eluant being CH2Cl2 /CH3OH/ammonium hydroxide (45:5:1), resulted in an oil which was dissolved in 50 ml of ethanol. Hydrogen chloride-saturated ether was added to this solution until the mixture tested acidic to litmus. The resulting precipitate was filtered off, dried and weighed to yield 5.6 g (68% of theory) of 1,3-bis[4-(3-chlorobenzyl)-1-piperazinyl]propane dihydrochloride monohydrate. Recrystallization from water gave a white crystalline solid (m.p. 248°-257° C., with decomp.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04725597 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-7341df2adb3541c79cb658048cb382de |
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| 출처 메모 | uspto-grants-1988_02 |
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