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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2354365생성일: 2026년 10월 25일

Trifluoroacetic acid → (6-Methoxy-2-oxo-benzooxazol-3-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/2354365

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Ethyl bromoacetateHCID 7748—
반응물CoixolHCID 10772—
반응물Sodium hydrideHCID 24758—
용매TetrahydrofuranHCID 8028—
용매Acetonitrile--water (1/1)HCID 18373917—
생성물(6-Methoxy-2-oxo-benzooxazol-3-yl)-acetic acid ethyl esterHCID 5743781381.4%

반응 단계

A solution of 6-methoxy-2-benzoxazolinone (0.78 g, 4.72 mmol) dissolved in 5 mL of anhydrous THF was added to a suspension of sodium hydride (0.208 g of a 60% dispersion in mineral oil, 5.2 mmol) in 10 mL of anhydrous THF at room temperature and stirred for 10 minutes. Then, ethyl bromoacetate (0.629 mL, 5.67 mmol) was added and stirred at room temperature for two hours. HPLC (Eclipse XDB-C18, 4.6×250 mm, 5 micron, 1-99% CH3CN/H2O with 0.1% trifluoroacetic acid) showed that almost all of the starting material (Rt=4.36 min) was gone and that a new peak (Rt=6.0 min) had formed. The reaction was quenched with 2 mL of 4.0M HCl in dioxane. The solvent was removed by rotary evaporation and the residue was adsorbed onto approximately 10 g of silica gel and purified by column chromatography (40 g silica gel 40 um, gradient elution from 100% dichloromethane to 35% methanol/65% dichloromethane over 40 minutes) to give ethyl[6-(methyloxy)-2-oxo-1,3-benzoxazol-3(2H)-yl]acetate (0.96 g, 3.84 mmol, 81%) as a white crystalline solid. MS (ES) m/e 252 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07749998B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-9d33237e732e4c5fac31da4d6f8a191e
출처 메모uspto-grants-2010_07