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Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Sodium 4-hydroxy-3-nitrobenzenesulfonate | HCID 12598197 | — |
| 反応物 | N-maleimido-6-aminocaproic acid | HCID 19361018 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N,N'-Dicyclohexylurea | HCID 4277 | — |
反応手順
One molar equivalent (2.24 g) of 4-hydroxy-3-nitrobenzene sulfonic acid sodium salt (HNSA) was mixed together with one molar equivalent (2.06 g) of dicyclohexylcarbodiimide and one molar equivalent (2.10 g) of N-maleimido-6-aminocaproic acid in 25 ml of dimethylformamide (DMF) at room temperature overnight. A white precipitate of dicyclohexyl urea was formed. The precipitate was filtered and 300 ml diethyl ether was added to the mother liquor. After about 10 minutes to 4 hours a gummy solid precipitated from the mother liquor was formed. This solid was found to contain 58% of active HNSA ester and 42% of free HNSA.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04762706 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-717c3c9f06e542e881321a78bdb17815 |
| 出典メモ | uspto-grants-1988_08 |