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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68255생성일: 2026년 10월 23일

Dichloromethane → 2-(Benzyl(methyl)amino)ethyl acetate

https://huagongshe.com/ko/reaction/68255

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물N-Benzyl-N-methylethanolamineHCID 66876—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매tert-Butyl methyl etherHCID 15413—
생성물2-(Benzyl(methyl)amino)ethyl acetateHCID 1476145487.5%

반응 단계

To a 500 mL dry round bottom flask were added 2-(benzyl(methyl)amino)ethanol (46.3 g, 280.2 mmol), triethylamine (150 mL, 1.08 mol), acetic anhydride (31.8 mL, 336.2 mmol), anhydrous CH2Cl2 (100 mL) and a crystal piece of DMAP (4-Dimethylaminopyridine). The mixture was stirred at room temperature for 3 hours. MTBE (700 mL) was added into the reaction mixture, and this mixture was washed, respectively, with cold 2N NaOH (150 mL), water (100 mL), brine (150 mL). The MTBE layer was concentrated, and the residue was poured onto a silica gel pad (200.0 g). The pad was eluted with a co-solvents of ethyl acetate: heptane=3:1 to give 2-(benzyl(methyl)amino)ethyl acetate (50.8 g) as a yellow oil. Yield: 87%. 1H NMR (CDCl3, 300 MHz): δ=7.41-7.25 (m, 5H), 4.29 (t, J=6.3 Hz, 2H), 3.65 (s, 2H), 2.74 (t, J=6.0 Hz, 2H), 2.38 (s, 3H), 2.14 (s, 3H). 13C NMR (CDCl3, 75.5 MHz): δ=170.9, 138.7, 128.9, 128.2, 127.1, 62.5, 62.2, 55.3, 42.6, 21.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822435B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-06eb02ba99414ce280872ed9b8f58245
출처 메모uspto-grants-2014_09