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HRID 327914作成日:2026年10月27日

Propionic Acid → 2-Propenoic acid, 3-(4-methoxyphenyl)-, 2-ethylhexyl ester

https://huagongshe.com/reaction/327914

反応式

関与物質

役割名称HCID仕込み量
反応物Propionic AcidHCID 1032—
反応物Sulfuric AcidHCID 1118—
反応物2-Ethylhexyl acrylateHCID 7636—
反応物P-AnisidineHCID 7732—
反応物Sodium HydroxideHCID 14798—
反応物Octane-3-yl acrylateHCID 15748566—
反応物Sodium NitriteHCID 23668193—
触媒Tert-ButylamineHCID 6385—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒WaterHCID 962—
生成物2-Propenoic acid, 3-(4-methoxyphenyl)-, 2-ethylhexyl esterHCID 2163094.1%

反応条件

温度0 °C

反応手順

p-Anisidine (123 g), propionic acid (200 ml) and water (250 ml) were mixed in a 5 liter reaction flask and cooled to 0° C. Sulfuric acid 98% (202 g) was added gradually with cooling followed by the addition of sodium nitrite (69 g) dissolved in 200 ml water over a 50 minute period. The stirring was continued for a further one hour at 0°-2° C., t-Butylamine (0.5 g) was then added. After an additional 15 minutes of stirring Pd(dba)2 (1.0 g) and propionic acid (250 ml) were added. 2-Ethylhexyl acrylate (276 g) was then added over a period of 10 minutes while maintaining the temperature at 0° C. The reaction was then allowed to warm to room temperature and stirred for 24 hours. Sodium hydroxide (333 g of 30% solution) was added and after 10 minutes the lower aqueous layer was separated and extracted twice with ether (200 ml). The ether layers were combined and evaporated. The residue was combined with the organic layer and distilled to give separate fractions of propionic acid, excess ethylhexyl acrylate and 273 g of 2-ethylhexyl p-methoxycinnamate (94.0% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05274171
出典データセットuspto-grants-1993_12
ORD IDord-ebf9ac92fe7b43f09b8521d638f9f1e8
出典メモuspto-grants-1993_12