関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Ethyl trans-4-Bromocinnamate | HCID 688115 | — |
| 反応物 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Propen-1-ol, 3-(4-bromophenyl)-, (2E)- | HCID 53396371 | — |
反応手順
To a solution of ethyl trans-4-bromocinnamate [CAS 24393-53-1] (8 mL, 42.6 mmol) in anhydrous dichloromethane (150 mL) under N2 was added dropwise diisobutylaluminum hydride in dichloromethane (128 mL, 1M, 128 mmol) at −78° C. Following the addition, the mixture was allowed to warm from −78° C. to −30° C. over two hours. The mixture was then cooled back to −78° C. and aqueous 1 N HCl was added. The organic layer was separated, dried with MgSO4, filtered and concentrated under reduced pressure to provide the title compound, 1H NMR (300 MHz, CDCl3): δ 1.44 (t, J=6 Hz, 1H), 4.32 (t, J=4.5 Hz, 2H), 6.37 (dt, J=16.5 Hz, J=6 Hz, 1H), 6.57 (dt, J=15 Hz, J=3 Hz, 1H), 7.25 (d, J=9 Hz, 2H), 7.45 (d, J=9 Hz, 2H). MS (DCl—NH3) m/z 214 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829041B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-a2ba5633355e4c80aa6763e8bda91d75 |
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| 出典メモ | uspto-grants-2014_09 |
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