戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 423028作成日:2026年10月27日

1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate → 1-tert-Butyl 4-ethyl 4-(aminomethyl)piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/423028

反応式

関与物質

役割名称HCID仕込み量
反応物1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylateHCID 57750376—
触媒Adams' catalystHCID 345198—
溶媒Acetic AcidHCID 176—
生成物1-tert-Butyl 4-ethyl 4-(aminomethyl)piperidine-1,4-dicarboxylateHCID 4683993583.1%

反応手順

Platinum(IV) oxide (0.724 g, 3.19 mmol) and 1-tert-butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate (Intermediate 7) (9 g, 31.9 mmol) in acetic acid (100 ml) were stirred under an atmosphere of hydrogen at 5 bar and 25° C. for 1 day. The crude product was filtered through celite and the filtrate purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and pure fractions were evaporated to dryness to afford 1-tert-butyl 4-ethyl 4-(aminomethyl)piperidine-1,4-dicarboxylate (7.59 g, 83%) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101623B2
出典データセットuspto-grants-2012_01
ORD IDord-b5b7caef13dc454ab83916b36337e3bb
出典メモuspto-grants-2012_01