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HRID 10178作成日:2026年10月25日

Trifluoroacetic acid → 1-Benzyl-3-(naphthalen-2-ylmethyl)piperazine

https://huagongshe.com/reaction/10178

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Ammonium HydroxideHCID 14923—
反応物4-Benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl esterHCID 21041081—
溶媒DichloromethaneHCID 6344—
生成物1-Benzyl-3-(naphthalen-2-ylmethyl)piperazineHCID 21978815—

反応手順

To a solution of 4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester (0.75 g) in dichloromethane (3 mL) was added dropwise trifluoroacetic acid (3 mL). After 75 min at room temperature the mixture was poured onto ice and made basic by the addition of ammonium hydroxide (25% solution). The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were dried over magnesium sulphate, filtered, and concentrated in vacuo to afford 1-benzyl-3-(naphthalen-2-ylmethyl)piperazine as an oil; 053 g (93%) MH+ 317, Rf 0.61 (CH2Cl2/MeOH/NH4OH 93/7/0.5), which was used as such.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094779B2
出典データセットuspto-grants-2006_08
ORD IDord-dbc56614992c4ee4a364e93a778a758a
出典メモuspto-grants-2006_08