참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 4-bromo-3-chloro-N-trimethylsilanylmethylthiobenzamide | HCID 86685705 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-bromo-3-chloro-N-trimethylsilanylmethyl-thiobenzimidic acid methyl ester | HCID 66836659 | 76.2% |
반응 단계
To a solution of 4-bromo-3-chloro-N-trimethylsilanylmethyl-thiobenzamide (10.40 g, 30.88 mmol) in THF (200 mL) was added methyl iodide (5.77 mL, 13.15 g, 92.7 mmol) and Cs2CO3 (30.19 g, 92.7 mmol) at −5° C. After 1 h at this temperature, the mixture was heated at 40° C. and stirred over night. Water was added and the mixture was extracted three times with MTBE. The combined organic phases were dried over Na2SO4, filtered and concentrated in vacuum. The residue was purified by filtration over a short plug of silica gel to give the title compound (8.25 g), which was used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08653000B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-c293342cb2f44c8c9470e59173be86d6 |
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| 출처 메모 | uspto-grants-2014_02 |
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