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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 577486생성일: 2026년 10월 23일

Triethylamine → N-(2,2-diethoxyethyl)-3-methoxy-2-nitrobenzamide

https://huagongshe.com/ko/reaction/577486

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물2,2-DiethoxyethylamineHCID 69524—
반응물3-Methoxy-2-nitrobenzoic acidHCID 78632—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-(2,2-diethoxyethyl)-3-methoxy-2-nitrobenzamideHCID 8672371297%

반응 단계

Oxalyl chloride (34 mL, 0.395 mol) was added to a solution of 3-methoxy-2-nitrobenzoic acid (60 g, 0.305 mol) in dry dichloromethane (600 mL), followed by N,N-dimethylformamide (0.6 mL, 7.8 mmol), which initiates mild gas evolution. The mixture was stirred at room temperature for two hours, then concentrated under vacuum to remove volatiles. The crude acid chloride was dissolved in dry dichloromethane (150 mL) then added dropwise to a cooled (5° C.) solution of aminoacetaldehyde diethylacetal (48 mL, 0.33 mol) and triethylamine (52 mL, 0.374 mol) in dry dichloromethane (250 mL). The mixture was stirred at room temperature for two hours, then washed with saturated aqueous sodium bicarbonate (2×100 mL) and brine (100 mL). The organics were dried over sodium sulfate and concentrated to give N-(2,2-diethoxyethyl)-3-methoxy-2-nitrobenzamide (296a, 92 g, 97% yield) as a yellow solid. MS: 335 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040515B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-3dd1029fa0c342ca8dc5e1dce0bb5721
출처 메모uspto-grants-2015_05