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HRID 894379作成日:2026年10月25日

Piperidine → Fenpropidin

https://huagongshe.com/reaction/894379

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Benzenepropanol, 4-(1,1-dimethylethyl)-beta-methyl-HCID 92013—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物FenpropidinHCID 9169494%

反応手順

A mixture of 153 parts of 3-p-tertiary butylphenyl-2-methyl-propanol, 70 parts of piperidine, 230 parts of methanol and 20 parts of catalyst, comprising 0.5% by weight of Pd and 5% by weight of Nd2O3 on Al2O3, is hydrogenated in a stirred autoclave of 1,000 parts by volume capacity, at 70° C. under a hydrogen pressure of 50 bar, until the pressure remains constant. The autoclave is then allowed to cool, the catalyst is filtered off and the filtrate is purified by distillation. 195 parts of N-(3'-(p-tertiary butylphenyl)-2'-methylpropyl)-piperidine, boiling point 117° C./0.2 mm Hg, are obtained. The yield is 94% of theory.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04283534
出典データセットuspto-grants-1981_08
ORD IDord-6cac709ee57a40e2a5318f5e20149460
出典メモuspto-grants-1981_08