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HRID 10273생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/10273

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Oxalyl chlorideHCID 65578—
반응물Sodium BicarbonateHCID 516892—
반응물2,4,5-Trifluoro-3-methoxybenzoic acidHCID 2733970—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Benzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl esterHCID 277438798.8%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094780B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-773f119220524fabb53ac3ee22baac20
출처 메모uspto-grants-2006_08