戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 17387作成日:2026年10月26日

Imidazole → 2-(tert-butyldiphenylsilyloxy)-N-methylethanamine

https://huagongshe.com/reaction/17387

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物2-(Methylamino)ethanolHCID 8016—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
溶媒DimethylformamideHCID 6228—
生成物2-(tert-butyldiphenylsilyloxy)-N-methylethanamineHCID 1182315839%

反応手順

Under nitrogen atmosphere, an N,N-dimethylformamide (33 ml) solution of tert-butylchlorodiphenylsilane (8.78 g, 32.0 mmol) was dropwise added at room temperature to an N,N-dimethylformamide (100 ml) solution of N-methylethanolamine (2.00 g, 26.6 mmol) and imidazole (2.72 g, 39.9 mmol), and stirred for 5.5 hours. The solvent was evaporated away under reduced pressure, then the residue was dissolved in ethyl acetate, and the solution was washed with saturated sodium hydrogencarbonate water, water and saturated brine. Next, the organic layer was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography, and the eluate with ethyl acetate gave the entitled compound (3.21 g, 39%) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737166B2
出典データセットuspto-grants-2010_06
ORD IDord-7114c87529a548ad8d6885f843c342be
出典メモuspto-grants-2010_06