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Benzyl Chloride → 1,1-di-(N-benzyl-indol-3-yl)-butane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Chloride | HCID 7503 | — |
| 反応物 | 3-[1-(1H-indol-3-yl)butyl]-1H-indole | HCID 10266133 | — |
| 触媒 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 溶媒 | Chloroform water | HCID 22418719 | — |
| 生成物 | 1,1-di-(N-benzyl-indol-3-yl)-butane | HCID 22019299 | 78% |
反応手順
ST 1385 1,1-di-indol-3-yl-butane, 290 mg (1 mmol), was thoroughly mixed and blended with potassium tertbutylate (280 mg) and tetrabutylammonium bromide (20 mg). The mixture thus obtained was held under ultrasonic stirring at ambient temperature. 640 mg (5 mmol) of benzylchloride at 0° C. were then added and the ultrasonic stirring was continued for 2 hours at room temperature. At the end of this period, the reaction mixture was treated with H2O/CHCl3; the chloroform phase was separated, washed with a small amount of water, dried on Na2SO4, filtered and concentrated to dryness. The end product was isolated and purified chromatographically on silica gel, eluting with hexane:ethyl ether 95:5.351 mg of product were obtained with a 78% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084166B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-4dd0bc4fe8c64d9e8f8801e446e2f232 |
| 出典メモ | uspto-grants-2006_08 |