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HRID 729362作成日:2026年10月27日

Ethanol → Benzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl ester

https://huagongshe.com/reaction/729362

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Oxalyl chlorideHCID 65578—
反応物Sodium BicarbonateHCID 516892—
反応物2,4,5-Trifluoro-3-methoxybenzoic acidHCID 2733970—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Benzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl esterHCID 277438798.8%

反応条件

温度0 °C

反応手順

A solution of 2,4,5-trifluoro-3-methoxybenzoic acid (2.513 g, 12.19 mmol) in dichloromethane (50 mL) at 0° C. is treated with oxalyl chloride (5.4 mL, 61.9 mmol) followed by N,N-dimethylformamide (4 drops). The mixture is stirred at 0° C. for 5 minutes and then at room temperature for 2.5 hours. The mixture is concentrated to near dryness and then co-evaporated from benzene. The resulting acid chloride is diluted with dichloromethane (50 mL), cooled to 0° C., and then anhydrous ethanol (7.30 mL, 124 mmol) is added dropwise. The resulting solution is stirred at room temperature for 4.5 hours, poured into saturated NaHCO3 solution, and extracted with dichloromethane. The combined organic extracts are washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to afford the title compound as a light yellow liquid (2.82 g). 1H NMR (CDCl3): δ 7.47 (ddd, 1H), 4.39 (q, 2H), 4.05 (s, 3H), 1.40 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582627B2
出典データセットuspto-grants-2009_09
ORD IDord-276df7c94fad4fc6a9035df569eaef47
出典メモuspto-grants-2009_09