関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | N,N-Diisopropyl-3-(2-thienyl)propenamide | HCID 4444087 | — |
| 反応物 | HCID 178506687 | HCID 178506687 | — |
| 溶媒 | Dimethyl Sulfide | HCID 1068 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | N,N-Diisopropyl-3-(2-methoxyphenyl)-3-(2-thienyl)propanamide | HCID 18357295 | — |
反応手順
Copper(I)bromide dimethyl sulfide complex (4.63 g 22.5 mmol) was dissolved in dimethyl sulfide (18 mL), and diethyl ether (15 mL). The solution was cooled to 0° C., whereafter 2-methoxyphenyllithium (41.2) (45 mmol) was added. After 10 min., the temperature was lowered to −78° C. Trimethylsilylchloride (4.89 g, 45.0 mmol) was added, followed by N,N-diisopropyl-3-(2-thienyl)propenamide (41.1) (3.56 g, 15 mmol) in diethyl ether (20 mL). The temperature was allowed to slowly rise to room temperature overnight. The reaction was quenched with saturated NH4Cl (10 mL) and conc. ammonia (10 mL). Diethyl ether (80 mL) was added and the mixture was filtered through Celite. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were washed once with brine and dried (MgSO4). The solvent was evaporated and the crude product was chromatographed on silica (petroleum ether-ethyl acetate 3:1), affording a yellow oil, 3.75 g (73%): 1H NMR (CDCl3) d 1.12 (t, 6H), 1.29 (t, 6H), 3.02 (m, 2H), 3.4 (br, 1H), 3.80 (s, 3H), 4.03 (m, 1H), 5.26 (t, 1H), 6.8-7.3 (m, 7H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06313132B1 |
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| 出典データセット | uspto-grants-2001_11 |
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| ORD ID | ord-7d8c3fcafa8c48e68ccc416205efb9e8 |
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| 出典メモ | uspto-grants-2001_11 |
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