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HRID 963652作成日:2026年10月26日

Toluene → 2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetal

https://huagongshe.com/reaction/963652

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物2,2-Dimethoxy-1-methylethylamineHCID 93658—
反応物4-(Benzyloxy)-2-chloro-1-nitrobenzeneHCID 819861—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetalHCID 19083116—

反応手順

A mixture of benzyl 3-chloro-4-nitrophenyl ether (48.2 g, 0.183 mole), 2-aminopropionaldehyde dimethyl acetal (65.3 g, 0.55 mole), potassium carbonate (101 g, 0.73 mole) and toluene in dry dimethyl sulfoxide, under nitrogen, is stirred at 99°-105° C. for 20 hours, cooled to room temperature and filtered. The filter cake is washed with ether. The combined filtrates are mixed with ice water. The phases are separated and the aqueous phase is extracted with ether. The ether extracts are combined with the organic phase. The combined organic phase is washed with six portions of water, dried (Na2SO4) and concentrated in vacuo to give an oil residue which is crystallized in methanol to afford the title product as a yellow solid, 39.6 g (64.5%). A sample is recrystallized from methanol to afford a yellow solid, mp 57°-62° C., identified by elemental and NMR analyses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763615
出典データセットuspto-grants-1998_06
ORD IDord-18fc9b6dbc484a6e8834325bb1a74df5
出典メモuspto-grants-1998_06