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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485284생성일: 2026년 10월 24일

Pyridine → 2-Nitrobenzeneacetaldehyde

https://huagongshe.com/ko/reaction/485284

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Trifluoroacetic acidHCID 6422—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-Nitrophenethyl alcoholHCID 27054—
반응물Oxalic acid dihydrateHCID 61373—
용매BenzeneHCID 241—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
용매Benzene ethyl acetateHCID 21583983—
생성물2-NitrobenzeneacetaldehydeHCID 1084476481%

반응 단계

Trifluoroacetic acid (1.31 ml, 17 mmols) and 2.7 ml (33.3 mmols) of pyridine were added to a mixture of 5.51 g (33.3 mmols) of 2-(2-nitrophenyl)ethanol, 50 ml of dimethyl sulfoxide, 50 ml of benzene and 21 g (0.1 mol) of DCC. After stirring the mixture at room temperature for 4 hours, 300 ml of aqueous solution of 8.82 g (70 mmols) of oxalic acid dihydrate was added thereto. The resulting mixture was stirred at room temperature for 30 minutes and diluted with 500 ml of ethyl acetate. The organic layer was separated off, washed with saturated NaCl, dried over Na2SO4 and concentrated to obtain a yellow oil. The oil was subjected to silica gel column chromatography (95:5 benzene-ethyl acetate) to obtain 2-nitrophenylacetoaldehyde in the form of an unstable oil in an amount of 4.50 g (yield 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04536391
출처 데이터셋uspto-grants-1985_08
ORD IDord-d91480da54914daba6ee0526fbba308a
출처 메모uspto-grants-1985_08