참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | 3-Bromo-1-(triisopropylsilyl)pyrrole | HCID 2763302 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(Triisopropylsilyl)pyrrole-3-boronic acid | HCID 2763303 | — |
반응 단계
To −78° C. solution of 3-bromo-1-(triisopropylsilyl)-1H-pyrrole (0.619 g, 2.288 mmol) in 10 mL THF was added tert-butyllithium (2.83 mL of 1.7 M in Heptane, 4.80 mmol) dropwise. The reaction mixture was stirring at −78° C. for 45 minutes, then trimethylborate (2.38 g, 22.88 mmol) was added. The reaction was stirred for another 45 minutes at −78° C. To this was then added 0.9 mL methanol and water solution (V/V=1:1) and the reaction was allowed warm to room temperature. The reaction mixture was quenched with H2O (30 mL), then extracted with EtOAc (3×30 mL) and the combined organic extracts washed with brine. The organic phase was dried over Na2SO4 and concentrated in vacuo, and used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07393959B2 |
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| 출처 데이터셋 | uspto-grants-2008_07 |
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| ORD ID | ord-f3c9ff7386824966b7599ee99336e74b |
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| 출처 메모 | uspto-grants-2008_07 |
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