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HRID 400431作成日:2026年10月26日

Methyl iodide → 1-tert-Butyl 4-methyl 4-methylpiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/400431

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物DiisopropylamineHCID 7912—
反応物1-N-Boc-4-Piperidinecarboxylic acid methyl esterHCID 392870—
溶媒TetrahydrofuranHCID 8028—
生成物1-tert-Butyl 4-methyl 4-methylpiperidine-1,4-dicarboxylateHCID 46318388—

反応条件

温度-78 °C

反応手順

137 mL Diisopropylamine in 3390 mL THF was cooled to 0° C. and 360 mL n-buthyllithium was added dropwise under nitrogen. The reaction was cooled to −78° C. and a solution of 180 mL piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-methyl ester in 1800 mL THF was added dropwise over 1 h. The reaction was stirred at −78° C. for 2 h and then 168 mL methyliodide in 300 mL THF was added in one portion. The mixture was stirred 2 h at −78° C. and then allowed to warm to RT. The reaction was quenched with saturated aqueous sodium sulfate solution, the organig phase was separated, dried and evaporated. The residue was purified by chromatography on silica gel to give 155 g of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741892B2
出典データセットuspto-grants-2014_06
ORD IDord-bb0709d09d8642869019a120a35b85a9
出典メモuspto-grants-2014_06