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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32159생성일: 2026년 10월 25일

Acetic Acid → 1-Butyl-4-(2-cyclooct-1-enylphenyl)piperazine

https://huagongshe.com/reaction/32159

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물ButanalHCID 261—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(2-Cyclooct-1-enylphenyl)piperazineHCID 69218982—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-Butyl-4-(2-cyclooct-1-enylphenyl)piperazineHCID 6921826274.5%

반응 단계

To a solution of 1-(2-cyclooct-1-enylphenyl)piperazine (11 mg, 0.0407 mmol) produced in Example (46a) in tetrahydrofuran (1 mL) were added butyraldehyde (0.0047 mL, 0.0529 mmol), sodium triacetoxyborohydride (11.2 mg, 0.0529 mmol) and acetic acid (0.0044 mL, 0.0773 mmol), followed by stirring for 14 hours and 20 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/heptane) to give 9.9 mg of 1-butyl-4-(2-cyclooct-1-enylphenyl)piperazine as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425554B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-13ec66df448c445f996b2d22352c8e59
출처 메모uspto-grants-2008_09