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HRID 840680作成日:2026年10月27日

Dimethyl Sulfate → N-Boc-2-Methyl-Piperidine

https://huagongshe.com/reaction/840680

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物N-(tert-butoxycarbonyl)piperidineHCID 7010304—
反応物CID 53628100HCID 178418400—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物N-Boc-2-Methyl-PiperidineHCID 457807799.2%

反応条件

温度-78 °C

反応手順

A solution of N-Boc-Piperidine (15.0 g, 80.95 mmol) in ether (160 mL) was cooled to −78° C. and treated with TMEDA (15.9 mL, 105.2 mmol) followed by sec-BuLi (85 mL, 105.2 mmol) dropwise. The mixture was stirred for 3 h at −78° C. and then treated with a solution of dimethyl sulfate (15.3 mL, 161.9 mmol) in 65 mL of ether. The mixture was warmed to room temperature and then was diluted with water and extracted with ether. The combined extracts were dried over K2CO3 and then concentrated to give a crude product as a colorless oil. The product was purified by column chromatography on silca gel with 5% EtOAc/hexane to afford 16.0 g (81%) of product as a clear oil which was homogeneous by TLC analysis. 1H NMR (300 MHz) 67 4.33 (m, 1 H), 3.92-3.81 (pair of br. d, 1 H), 2.81-2.72 (dt, 1H), 1.60-1.36 (m, 15 H), 1.09-1.07 (d, 3 H); 13C NMR (75 MHz) 154.9 (s), 78.6 (s), 45.9 (s), 38.6 (s), 29.9 (s), 28.4 (s), 25.6 (s), 18.6 (s), 15.6 (s), ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06369078B1
出典データセットuspto-grants-2002_04
ORD IDord-04bcec3d8e0849d38352a346ae5610cd
出典メモuspto-grants-2002_04