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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515104생성일: 2026년 10월 25일

Trifluoroacetic acid → 5-Bromo-4-methylisobenzofuran-1(3H)-one

https://huagongshe.com/reaction/515104

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Lithium ChlorideHCID 433294—
반응물Magnesium monoxideHCID 6850729—
반응물(3-Bromo-2-methylphenyl)methanolHCID 10035697—
반응물Thallium(1+);2,2,2-trifluoroacetateHCID 21902506—
촉매Palladium ChlorideHCID 24290—
용매MethanolHCID 887—
생성물5-Bromo-4-methylisobenzofuran-1(3H)-oneHCID 59568711—

반응 단계

To a flask charged with (3-bromo-2-methylphenyl)methanol (6.0 g, 30 mmol) was added a 1M trifluoroacetic acid solution of thallium trifluoroacetate (16.2 g, 29.8 mmol). The mixture was stirred at room temperature overnight. The solvent was removed under vacuum, and the residue was pumped under high vacuum for 30 minutes to ensure complete removal of TFA. To the residue was then added palladium(II) chloride (529 mg, 2.98 mmol), lithium chloride (2.53 g, 59.7 mmol), magnesium oxide (2.41 g, 59.7 mmol), and methanol (150 mL). The reaction was flushed with CO twice, and kept under CO at room temperature. Analysis by LC showed a big product spot within 2 hours. To this solution was added ethyl acetate to precipitate the salts. The black solution was filtered through a Celite® diatomaceous earth pad, washed with EtOAc, adsorbed onto silica and purified by silica gel chromatography to afford 5-bromo-4-methyl-2-benzofuran-1(3H)-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108947B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-6ad1df555dff48b984da1361189e59aa
출처 메모uspto-grants-2015_08