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Acetone → 1-(6-Bromoquinoline-2-yl)-2-methylpropane-2-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | 6-Bromo-2-methylquinoline | HCID 522885 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-(6-Bromoquinoline-2-yl)-2-methylpropane-2-ol | HCID 23158227 | — |
反応手順
20 ml of diethylether was added to 2.22 g of 6-bromoquinaldine, and 3.76 ml of 2.66 M normal butyl lithium was dropped thereto at −78° C. The obtained suspension was stirred for 5 min, 2 ml of anhydrous acetone was added and the mixture was further stirred for 10 min, and water was added. The products were extracted with ethyl acetate, organic layer was dried with anhydrous sodium sulfated and the solvents were distilled outunder reduced pressure. The obtained residues were separated and purified by silicagel colum chromatography (hexane:ethyl acetate=2:1) to obtain 1.14 g of the above compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07902369B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-a056bae2b55a41a387e3634c7b8d9f63 |
| 出典メモ | uspto-grants-2011_03 |