戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1154728作成日:2026年10月26日

Methanol → Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-

https://huagongshe.com/reaction/1154728

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物1-(4-Methoxyphenyl)-4-(4-nitrophenyl)piperazineHCID 5134657—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-HCID 15440674%

反応手順

A mixture of 12 parts of 1-(4-methoxyphenyl)-4-(4-nitrophenyl)piperazine, 200 parts of methanol and 225 parts of tetrahydrofuran is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and washed with N,N-dimethylacetamide. The filtrate is poured onto water. The precipitated product is filtered off and crystallized from 1-butanol, yielding 8 parts (74%) of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine; mp. 191.8° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04490530
出典データセットuspto-grants-1984_12
ORD IDord-25c3423e6e894d7bb0b00ccbd2a57ac2
出典メモuspto-grants-1984_12