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HRID 515104作成日:2026年10月26日

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

https://huagongshe.com/reaction/515104

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Lithium ChlorideHCID 433294—
反応物Magnesium monoxideHCID 6850729—
反応物(3-Bromo-2-methylphenyl)methanolHCID 10035697—
反応物Thallium(1+);2,2,2-trifluoroacetateHCID 21902506—
触媒Palladium ChlorideHCID 24290—
溶媒MethanolHCID 887—
生成物5-Bromo-4-methylisobenzofuran-1(3H)-oneHCID 59568711—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108947B2
出典データセットuspto-grants-2015_08
ORD IDord-6ad1df555dff48b984da1361189e59aa
出典メモuspto-grants-2015_08