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HRID 277750作成日:2026年10月27日

Acetic Acid → 1-Cyclohexyl-4-(4-(2-methoxyphenyl)piperazin-1-yl)-2-methyl-2-phenylbutan-1-one

https://huagongshe.com/reaction/277750

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Sodium triacetoxyborohydrideHCID 5049666—
反応物N-(2-Methoxyphenyl)piperazine hydrochlorideHCID 9899402—
反応物4-Cyclohexyl-3-methyl-4-oxo-3-phenylbutanalHCID 11780192—
溶媒DichloromethaneHCID 6344—
生成物1-Cyclohexyl-4-(4-(2-methoxyphenyl)piperazin-1-yl)-2-methyl-2-phenylbutan-1-oneHCID 9802987—

反応手順

3-Phenyl-3-cyclohexanecarbonyl-butan-1-al (57.8 g, 224 mmol) was dissolved in methylene chloride (1650 mL) followed by addition of 1-(2-methoxyphenyl)piperazine hydrochloride (56.3 g, 246 mmol). Acetic acid (41 mL) may optionally be added to turn the slurry into a solution. To the stirred solution, sodium triacetoxyborohydride (60.3 g, 284 mmol)was slowly added. A slight exotherm resulted and a slurry was produced. The reaction mixture was stirred for an additional 3 hours at room temperature. The reaction was then quenched by addition of 2.0 N sodium hydroxide (1050 mL) producing a pH of about 10 for the quenched reaction mixture. The mixture was then extracted with methylene chloride (2 times, 1L and 300 mL). The organic extracts were combined, washed successively with 1.0 N HCl (600 mL), 1.0 N sodium hydroxide (600 mL), brine (600 mL), dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum to provide the final title compound as a thick oil;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358958B2
出典データセットuspto-grants-2002_03
ORD IDord-a2905979d8b5472281c54a246be2e02b
出典メモuspto-grants-2002_03