Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32177생성일: 2026년 10월 23일
Tri-tert-butylphosphine tetrafluoroborate → 1-[4-Azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine
https://huagongshe.com/ko/reaction/32177
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| 반응물 | Azetidine hydrochloride | HCID 12308726 | — |
| 반응물 | 1-[4-Bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine | HCID 23141738 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-[4-Azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine | HCID 59769431 | — |
반응 단계
A mixture of 1-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine (50 mg, 0.123 mmol) produced in Example (57b), azetidine hydrochloride (17 mg, 0.185 mmol), sodium t-butoxide (47 mg, 0.492 mmol), palladium(II) acetate (3 mg, 0.0123 mmol), tri-t-butylphosphonium tetrafluoroborate (11 mg, 0.0369 mmol) and xylene (1 mL) was stirred for 3 hours at an external temperature of 100° C. Water was added to the reaction mixture and extraction was performed with ethyl acetate. The separated organic layer was filtered through Celite. The solvent was distilled off by nitrogen stream to the filtrate. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/hexane) to give 1-[4-azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine as a colorless solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07425554B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-33f191f7e03346e3b882e7d82f26d813 |
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| 출처 메모 | uspto-grants-2008_09 |
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