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HRID 745486作成日:2026年10月25日

Benzyl Bromide → 1-Methyl-1-benzyl-4-[3-(4-tert.-butylphenyl)-2-methylpropyl]-piperazinium bromide

https://huagongshe.com/reaction/745486

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物1-[3-(4-tert-Butylphenyl)-2-methylpropyl]-4-methylpiperazineHCID 13251981—
溶媒Ethyl AcetateHCID 8857—
生成物1-Methyl-1-benzyl-4-[3-(4-tert.-butylphenyl)-2-methylpropyl]-piperazinium bromideHCID 1325198280.2%

反応手順

A solution of 14.4 g of 1-methyl-4-[3-(4-tert.-butylphenyl)-2-methylpropyl]-piperazine and 10.3 g of benzyl bromide in 200 ml of ethyl acetate was refluxed for 6 hours, after which the mixture was evaporated down to 80 ml and then cooled to +5° C. The precipitated product was filtered off under suction, washed with ether and dried. 18.4 g of 1-methyl-1-benzyl-4-[3-(4-tert.-butylphenyl)-2-methylpropyl]-piperazinium bromide were obtained in the form of colorless crystals of melting point 216° C. (compound 3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04599335
出典データセットuspto-grants-1986_07
ORD IDord-bd19a1f8882144ec99b21925d36208f7
出典メモuspto-grants-1986_07