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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32164생성일: 2026년 10월 23일

Acetic Acid → 1-Cyclopentyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

https://huagongshe.com/ko/reaction/32164

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물CyclopentanoneHCID 8452—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
용매Ethyl AcetateHCID 8857—
생성물1-Cyclopentyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 23141649—

반응 단계

A mixture of 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (25 mg, 0.0832 mmol) produced in Example (8b), cyclopentanone (9.1 mg, 0.108 mmol), sodium triacetoxyborohydride (33.5 mg, 0.158 mmol) and acetic acid (0.009 mL, 0.158 mmol) was stirred for 1 hour and 40 minutes at room temperature. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed three times with ethyl acetate. The organic layer was concentrated to produce a residue, which was purified by NH silica gel column chromatography (ethyl acetate/hexane) to give 1-cyclopentyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine as a colorless oil. δ: 0.92 (s, 6H), 1.13 (s, 6H), 1.16-1.36 (m, 6H), 1.39-1.51 (m, 4H), 1.66-1.76 (m, 2H), 1.86-1.96 (m, 2H), 2.48-2.58 (m, 1H), 2.67 (brs, 4H), 2.89-2.98 (m, 4H), 3.52-3.61 (m, 1H), 7.04-7.14 (m, 3H), 7.21 (d, J=8.8 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425554B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f7cec2cd12ba4e52b0f7a2ba31ebc45d
출처 메모uspto-grants-2008_09