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Dimethylformamide → 1-Chloro-3,4-dihydronaphthalene-2-carboxaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 1-Tetralone | HCID 10724 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 生成物 | 1-Chloro-3,4-dihydronaphthalene-2-carboxaldehyde | HCID 76752 | — |
反応手順
To N,N-dimethylformamide (2.3 mL) at 0° C. was added phosphorus oxychloride (2.33 mL) dropwise and the solution stirred at ambient temperature for 30 minutes. To this solution was added 3,4-dihydronaphthalen-1(2H)-one (1.46 g) and the mixture heated to 45° C. for 1 hour. The mixture was quenched with ice and extracted with diethyl ether. The combined organic layers were washed with water, saturated sodium bicarbonate, and water, dried over magnesium sulfate, filtered, and concentrated to provide 1.9 g of the title compound as a yellow oil, which was used without further purification. 1H NMR (DMSO-d6) δ 10.28 (s, 1H), 7.81-7.84 (m, 1H), 7.33-7.50 (m, 3H), 2.82-2.87 (m, 2H), 2.54-2.57 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08148384B2 |
| 出典データセット | uspto-grants-2012_04 |
| ORD ID | ord-3fc42c33eeea4a0889ff1bd9aa5e0450 |
| 出典メモ | uspto-grants-2012_04 |