関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Dioctylamine | HCID 3094 | — |
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-Allyl-N,N-di-n-octylamine | HCID 4562804 | — |
反応手順
Vinylsulfomethylpolystyrene resin 3 (0.42 mmol g−1 (est), 160 mg) in DMF (2 cm3) was treated with dioctylamine (1.7 mmol, 515 mm3) at 20° C. for 24 h. The resin was washed with DMF (10×5 cm3) and DCM (10 cm3), resuspended in DMF (2 cm3) and treated with allyl bromide (4.25 mmol, 365 mm3) at 20° C. for 24 h. The solvent and the reagent was then removed by filtration and the resin washed with DCM (2×20 cm3). The elimination was performed in DCM (4 cm3) with DIEA (1.72 mmol, 300 mm3) overnight. The filtrate of this last reaction step was combined with the DCM and MeOH, washed (25 cm3) from the resin and evaporated. It gave 14 contaminated with DIEA in 38 mg yield. The amine was transferred in a little DCM (<5 cm3) to a K2CO3 covered dry silica column (5 g). Impurities were washed away with hexane and the amine eluted with ethyl acetate. After the removal of the solvent 14 was obtained as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06486354B1 |
|---|
| 出典データセット | uspto-grants-2002_11 |
|---|
| ORD ID | ord-16cd478fae0741f69f5e2b4551b2edea |
|---|
| 出典メモ | uspto-grants-2002_11 |
|---|