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HRID 32159作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/32159

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物ButanalHCID 261—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-(2-Cyclooct-1-enylphenyl)piperazineHCID 69218982—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-Butyl-4-(2-cyclooct-1-enylphenyl)piperazineHCID 6921826274.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-13ec66df448c445f996b2d22352c8e59
出典メモuspto-grants-2008_09