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Triethylamine → 4-Bromo-1-(octahydroquinolin-1-yl)butan-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Decahydroquinoline | HCID 92911 | — |
| 反応物 | 5-Bromovaleryl chloride | HCID 521173 | — |
| 生成物 | 4-Bromo-1-(octahydroquinolin-1-yl)butan-1-one | HCID 66794644 | — |
反応手順
1.37 mL (9.9 mmol) of Et3N and 0.5 mL (4.5 mmol) of 5-bromovaleric acid chloride are added to a solution of 1 mL (4.0 mmol) of the decahydroquinoline in AcOEt. The resulting solution is kept under stirring for 18 h at rt. The solution is then washed with water, and the water re-extracted twice with AcOEt. The pooled organic phases are sequentially washed with 5% solution of NaHCO3, 1N HCl and saturated ammonium chloride solution. Finally the organic phase is dried over anhydrous Na2SO4, it is filtered and the solvent is evaporated under reduced pressure. 1.2 g of a yellow oil, which was used without subsequent purification, are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524894B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-4385fe3b05a5409db891b352d1f7b58c |
| 出典メモ | uspto-grants-2013_09 |