関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodoethane | HCID 6340 | — |
| 反応物 | N-(4-Butyrylphenyl)acetamide | HCID 4304236 | — |
| 反応物 | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-(4-(2-ethylbutanoyl)phenyl)acetamide | HCID 43160160 | — |
反応手順
To a solution of N-(4-butyrylphenyl)acetamide (3 g, 14.6 mmol) in THF (300 mL) was added 2.0 M LDA THF (18.3 mL) at −78° C. and then the reaction mixture was stirred for 1 h at −78° C. Iodoethane was added and stirred overnight at RT. The reaction mixture was quenched with sat. aq. NH4Cl and then extracted with ethyl acetate. The combined organic layers were dried over MgSO4, filtered and then concentrated. The crude product was purified by preparative TLC using 50% ethyl acetate in hexane as eluent to afford N-(4-(2-ethylbutanoyl)phenyl)acetamide as white solid. MS (ES+): m/z 234.28 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08865752B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-fecdf382f0564c6ebddbfea5285b64fe |
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| 出典メモ | uspto-grants-2014_10 |
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