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HRID 32135作成日:2026年10月24日

Acetic Acid → 1-[2-(4,4-Dimethylcyclohex-1-enyl)-5-methoxyphenyl]-4-pentylpiperazine

https://huagongshe.com/ja/reaction/32135

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PentanalHCID 8063—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-[2-(4,4-Dimethylcyclohex-1-enyl)-5-methoxyphenyl]piperazineHCID 23142046—
溶媒TetrahydrofuranHCID 8028—
生成物1-[2-(4,4-Dimethylcyclohex-1-enyl)-5-methoxyphenyl]-4-pentylpiperazineHCID 23141862102.4%

反応手順

To a solution of 1-[2-(4,4-dimethylcyclohex-1-enyl)-5-methoxyphenyl]piperazine (90 mg, 0.29 mmol) prepared in Example (1e) in tetrahydrofuran (10 mL) were added valeraldehyde (31 mg, 0.36 mmol), sodium triacetoxyborohydride (95 mg, 0.59 mmol) and acetic acid (35 mg, 0.59 mmol) in that order, and the mixture was stirred for 3 hours. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, the desiccant was filtered off and then the filtrate was concentrated under reduced pressure. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/hexane) to give 110 mg of 1-[2-(4,4-dimethylcyclohex-1-enyl)-5-methoxyphenyl]-4-pentylpiperazine as a light yellow 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-3af5112db2a047519e77a00c64bfd1a6
出典メモuspto-grants-2008_09