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HRID 441879作成日:2026年10月26日

Piperidine → Ethyl 2-methyl-4-piperidinobutyrate

https://huagongshe.com/reaction/441879

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Ethyl 4-bromo-2-methylbutanoateHCID 12780980—
溶媒BenzeneHCID 241—
生成物Ethyl 2-methyl-4-piperidinobutyrateHCID 20361120—

反応条件

温度60 °C

反応手順

10.5 g. (0.05 mole) of ethyl γ-bromo-α-methylbutyrate was combined with 17.0 g. (0.20 mole) of piperidine and 100 ml. of benzene and stirred for 16 hours at room temperature and heated at 60° C. for 4 hours. The reaction mixture was cooled and the colorless solid which appeared was removed by filtration. The mother liquor was concentrated to give ethyl α-methyl-γ-piperidinobutyrate as a mobile yellow liquid which distilled (b.p. 78° C. at 0.25 mm.) as 6.7 g. (63%) of colorless liquid. The nuclear magnetic resonance and infrared spectra were consistent with the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04042694
出典データセットuspto-grants-1977_08
ORD IDord-5285d10f4538403f9ea38ebefec88d98
出典メモuspto-grants-1977_08