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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

반응식

참여 물질

역할이름HCID투입량
반응물Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
반응물Azetidine hydrochlorideHCID 12308726—
반응물1-[4-Bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazineHCID 23141738—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매O-XyleneHCID 7237—
용매Ethyl AcetateHCID 8857—
생성물1-[4-Azetidin-1-yl-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazineHCID 59769431—

반응 조건

온도100 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425554B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-33f191f7e03346e3b882e7d82f26d813
출처 메모uspto-grants-2008_09