참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | Magnesium monoxide | HCID 6850729 | — |
| 반응물 | (3-Bromo-2-methylphenyl)methanol | HCID 10035697 | — |
| 반응물 | Thallium(1+);2,2,2-trifluoroacetate | HCID 21902506 | — |
| 촉매 | Palladium Chloride | HCID 24290 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 5-Bromo-4-methylisobenzofuran-1(3H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09108947B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-6ad1df555dff48b984da1361189e59aa |
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| 출처 메모 | uspto-grants-2015_08 |
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