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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366744생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/366744

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Sodium hydrideHCID 24758—
반응물tert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물tert-butyl N-ethyl-N-(prop-2-yn-1-yl)carbamateHCID 18366151—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06130239
출처 데이터셋uspto-grants-2000_10
ORD IDord-315fa2a1807f4e388b12c471ce453f26
출처 메모uspto-grants-2000_10