HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569854Generated: October 31, 2026
Ethylmorpholine → HCID 14181588, compound
https://huagongshe.com/reaction/569854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Cyclopentanecarboxylic acid | HCID 18840 | — |
| Reactant | HCID 86742072 | HCID 86742072 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14181588 | HCID 14181588 | — |
Reaction Steps
A cool solution of 15 mmoles of dicyclohexylcarbodiimide in dichloromethane is added to a solution of 15 mmoles of cyclopentanecarboxylic acid in dichloromethane, at -5° C. 15 mmoles of norvaline benzyl ester toluenesulfonate salt in dimethylformamide (DMF), which is neutralized with N-ethyl morpholine, is then added. The reaction mixture is stirred at 0° C. initially and then at room temperature until the reaction is completed as judged by TLC. Dicyclohexylurea is removed by filtration and 50 ml of ethyl acetate is added to the filtrate. The organic phase is washed until neutral, dried over anhydrous MgSO4 and filtered. The solvent is removed with a rotary evaporator. The residue is crystalized from isopropanol and hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04734420 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-b53a188d7d65495780b86e4d39c18034 |
|---|
| Source note | uspto-grants-1988_03 |
|---|