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HRID 485284作成日:2026年10月26日

Pyridine → 2-Nitrobenzeneacetaldehyde

https://huagongshe.com/reaction/485284

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Trifluoroacetic acidHCID 6422—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物2-Nitrophenethyl alcoholHCID 27054—
反応物Oxalic acid dihydrateHCID 61373—
溶媒BenzeneHCID 241—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
溶媒Benzene ethyl acetateHCID 21583983—
生成物2-NitrobenzeneacetaldehydeHCID 1084476481%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04536391
出典データセットuspto-grants-1985_08
ORD IDord-d91480da54914daba6ee0526fbba308a
出典メモuspto-grants-1985_08