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HRID 1069766作成日:2026年10月26日

Iodoethane → tert-butyl N-ethyl-N-(prop-2-yn-1-yl)carbamate

https://huagongshe.com/reaction/1069766

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Sodium hydrideHCID 24758—
反応物tert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物tert-butyl N-ethyl-N-(prop-2-yn-1-yl)carbamateHCID 18366151—

反応手順

Di-tert-butyl dicarbonate (42.8 g, 196 mmol) in dichloromethane (100 mL) was added dropwise to a solution of propargylamine (11.02 g, 200 mmol) in dichloromethane (200 mL) at room temperature with magnetic stirring. After 2 h, the reaction mixture was washed with aqueous 1N hydrochloric acid (300 mL) and saturated aqueous sodium bicarbonate solution (300 mL). The aqueous layers were washed with dichloromethane (300 mL). The dichloromethane solutions were combined, dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography (Biotage 40S, EtOAc—hexanes V/V 1:9 as solvent) to give crude N-Boc-propargyl amine. (32.32 g). The crude N-Boc-propargyl amine (3.1 g, 20 mmol) was dissolved in dry dimethylformamide (20 mL) with magnetic stirring and cooled in an ice—water bath. Sodium hydride (0.61 g, 24 mmol) was added in small portions. After stirring for 15 min., iodoethane (3.74 g, 24 mmol) was added. The mixture was allowed to warm to room temperature and stirred for 3 h. then diluted with ether and extracted with water and saturated brine. The aqueous layers were back washed with ether and the ether layers were combined, dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography (Biotage 40M, ethyl acetate—hexanes as solvent to give N-Boc-N-ethylpropargyl amine. (Yield 3.19 g, 87%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06252086B1
出典データセットuspto-grants-2001_06
ORD IDord-bdc4396197124488a36b7e6a28910aa3
出典メモuspto-grants-2001_06