참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Bromo-2-fluorobenzaldehyde | HCID 22019361 | — |
| 반응물 | HCID 178418255 | HCID 178418255 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (3-Bromo-2-fluorophenyl)(phenyl)methanol | HCID 71743205 | — |
반응 단계
To a solution of 3-bromo-2-fluorobenzaldehyde (0.150 g, 0.739 mmol) in THF (3.21 mL) cooled to −78° C. was added phenylmagnesium bromide (0.887 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr and then allowed to warm to room temperature slowly over 3 hr. The reaction was quenched with a saturated aqueous solution of NH4Cl. The reaction mixture was diluted with CH2Cl2 and the layers were separated. The aqueous phase was extracted twice with CH2Cl2. The organic layers were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a colorless residue.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09242967B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-32a24a7b571145808c77e56cb979c56b |
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| 출처 메모 | uspto-grants-2016_01 |
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