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HRID 9753作成日:2026年10月23日

Acetic Acid → 4-Nitrobenzaldehyde

https://huagongshe.com/ja/reaction/9753

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-NitrotolueneHCID 7473—
反応物1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trioneHCID 10419723—
触媒Cobalt diacetateHCID 6277—
触媒Manganous AcetateHCID 12525—
溶媒WaterHCID 962—
生成物4-NitrobenzaldehydeHCID 541—
生成物4-Nitrobenzoic AcidHCID 6108—

反応条件

温度130 °C

反応手順

In an autoclave, 0.274 g of 4-nitrotoluene, 0.011 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (3% by mole relative to 4-nitrotoluene), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4H2O and 0.001 g of manganese(II) acetate.4H2O were placed. The autoclave was charged with 1 MPa of air and placed in a heated oil bath. The mixture was stirred at 130° C. for 14 hours. After the completion of reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by gas chromatography and was found to yield 4-nitrobenzoic acid and 4-nitrobenzaldehyde in 85% and 1% yields, respectively, at 91% conversion of 4-nitrotoluene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091342B2
出典データセットuspto-grants-2006_08
ORD IDord-f7323dbcef384483968c17fe3f4b0f01
出典メモuspto-grants-2006_08