HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 53860365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1-{[(Benzyloxy)carbonyl]amino}cyclopropane-1-carboxylic acid | HCID 3589012 | — |
| Reactant | 2,2,5,5-Tetramethylcyclopentanamine | HCID 13247939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53860365 | HCID 53860365 | — |
Reaction Steps
To a stirred solution of N-Cbz-1-aminocyclopropanecarboxylic acid in dry CH2Cl2 containing dicyclohexylcarbodiimide and dimethylaminopyridine (DMAP), all at 0° C., is added, via an addition funnel, 2,2,5,5-tetramethyl-1-cyclopentyl amine dissolved in CH2Cl2. After stirring for 48 hours, the mixture is filtered, and the filtrate is washed with 5% HCl (1×50 ml), saturated NaHCO3 (1×50 ml), and water (2×50 ml). The organic layer is separated, dried over MgSO4 and evaporated to yield N-Cbz-1-aminocyclopropanecarboxylic acid 2,2,5,5-tetramethylcyclopentyl amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04572799 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-14514bb1f915429d878a5c48809805e9 |
| Source note | uspto-grants-1986_02 |