戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 46446作成日:2026年10月24日

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/ja/reaction/46446

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 89529—
溶媒Dioxane tetrahydrofuranHCID 22018518—
生成物N,N'-DicyclohexylureaHCID 4277—
生成物3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 89529—

反応手順

The N-hydroxy-5-norbornene-2,3-dicarboximide active ester of N-benzyloxycarbonyl DL-2-hydroxy-4-aminoburyric acid was prepared according to the procedure of M. Fujino, et al [Chem. Pharm. Bull. Japan, 22, 1857 (1974)]. To an ice cold solution of 0.40 g. of N-benzyloxycarbonyl-DL-2-hydroxy-4-aminoburyric acid and 0.32 g. of N-hydroxy-5-norbornene-2,3-dicarboximide in 3 ml. of tetrahydrofuran-dioxane (1:1 v/v), there was added, with stirring, 0.36 g. of N,N'-dicyclohexylcarbodiimide and 1 ml. of the above solvent mixture. The solution was stirred in the cold for 30 minutes and then at room temperature for 2 hours. The N,N'-dicyclohexylurea which formed in the above reaction was collected on a filter and washed with three 1-ml. portions of tetrahydrofuran-dioxane (1:1 v/v).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04173564
出典データセットuspto-grants-1979_11
ORD IDord-2cee5217ac594719a7c75f155a181beb
出典メモuspto-grants-1979_11