참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(5-Bromopyrimidin-2-yl)ethan-1-one | HCID 53488064 | — |
| 반응물 | HCID 178418689 | HCID 178418689 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(5-Bromopyrimidin-2-yl)propan-2-ol | HCID 58485286 | 46.77% |
반응 단계
To a solution of 1-(5-bromopyrimidin-2-yl)ethanone (99 mg, 0.50 mmol) in THF (10 mL) was added MeMgBr (1.65 mL, 4.95 mmol) at −78° C. under nitrogen. The formed solution was stirred at −78° C. for 20 min, quenched with satd aq NH4Cl, and extracted with EtOAc. The combined organic layer was dried over anhydrous Na2SO4 and concentrated to give an oil, which was purified by prep TLC (3:1 PE/EtOAc) to give 2-(5-bromopyrimidin-2-yl)propan-2-ol (50 mg, yield: 46.77%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08569292B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-6601085bd313461aa1c2e3612db19e05 |
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| 출처 메모 | uspto-grants-2013_10 |
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