참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethyl 3-bromo-4-cyanobenzoate | HCID 18374323 | — |
| 반응물 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Bromo-4-(hydroxymethyl)benzaldehyde | HCID 18374372 | 83% |
반응 단계
To a stirring cold (−78° C.) solution of ethyl 3-bromo-4-cyanobenzoate (0.41 mol, 104 g) in THF (2.3 L was added dropwise a solution of diisobutylaluminum hydride (2.0 mol, 1.36 L; 1.5 M in toluene) over a period of 1.5 h. After addition was completed, the mixture was warmed to rt over a period of 3 h. The mixture was then cooled to 0–5° C. and 40 ml of acetone was added slowly. The mixture was then transferred via a cannula to a cold (0° C.) stirring aqueous solution of HCl (2.2 L 3 N) over a period of 1.5 h, maintaining the temperature of the aqueous solution below 30° C. After the transfer was completed, the mixture was stirred for another 0.25 h. The organic solution was separated and the aqueous was extracted twice with EtOAc (3 L). The combined organic extracts were washed with brine, dried with MgSO4 (anhyd.) and concentrated to give 74 g (83%) of the title compound as a light yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07163932B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-010c517dda5a4ba389f59be0c340c17c |
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| 출처 메모 | uspto-grants-2007_01 |
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