関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Butylamine | HCID 8007 | — |
| 反応物 | Tetramethylurea | HCID 12437 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | N''-Butyl-N,N,N',N'-tetramethyl-guanidine | HCID 525255 | — |
反応手順
N,N,N′,N′-tetramethyl-N″-butylguanidine was prepared as follows: 9.3 g tetramethyl urea was added to 80 mL dry dichloroethane in a two-neck 250 mL round-bottom-flask. 11.3 mL oxalyl chloride was added and the solution was heated at 70° C. for two hours. The solvent was evaporated in vacuo after the solution cooled to room temperature. Residual solid was then dissolved in dry acetonitrile and cooled to 0° C. 15 mL butyl amine (1.02 eq) was slowly added. The solution was slowly warmed and allowed to reflux for one hour. Finally, the mixture was cooled to room temperature and the solvent was removed in vacuo to yield 9 g of a clear oil. 1H (CDCl3): δ (ppm): 2.99 (t, 2H); 2.62 (s, 3H); 2.53 (s, 3H); 1.39 (quintet, 2H); 1.24 (quintet, 2H); 0.78 (t, 3H). The synthesis was performed several times and the yield ranged from 37%-70%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07982069B2 |
|---|
| 出典データセット | uspto-grants-2011_07 |
|---|
| ORD ID | ord-ed7d99adbcfb4e95a443846a6fc3f023 |
|---|
| 出典メモ | uspto-grants-2011_07 |
|---|