関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methacryloyl chloride | HCID 13528 | — |
| 反応物 | 2-Butenamide | HCID 5354487 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | (E)-N-methacryloylbut-2-enamide | HCID 72205393 | — |
反応手順
Experimental Procedure: To a suspension of (E)-but-2-enamide (1.0 equiv) in 3.5 mL THF was added n-BuLi in hexanes (2.5 M,1.2 equiv) slowly at −78° C. The reaction mixture was warmed up to room temperature and stirred for 8 h before a solution of methacryloyl chloride (2.0 equiv) in 2 mL of THF was added drop wise at −78° C. The reaction mixture was allowed to warm up to rt overnight. The crude reaction mixture was diluted with ethyl acetate, and quenched with cold NH4Cl(aq, sat), and the organic layer separated. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with brine and dried over MgSO4. After filtration and evaporation under reduced pressure, the residue was purified by column chromatography to yield the pure compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09108923B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-b6e713ba9a044e2b97d5ba2a0a95dbc8 |
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| 出典メモ | uspto-grants-2015_08 |
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