HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → (2R)-1-(tert-butoxycarbonyl)-4-ethylpiperazine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2R)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acid | HCID 24820285 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2R)-1-(tert-butoxycarbonyl)-4-ethylpiperazine-2-carboxylic acid | HCID 59846012 | — |
Reaction Steps
To (2R)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (1.406 g) and Na2CO3 (2.59 g) was added dry EtOH (28 ml) then ethyl iodide (0.54 ml) and the mixture heated at reflux for 18 h under argon. The solvent was then removed under reduced pressure and 5% MeOH/DCM (40 ml) was added and stirred for 1 hour in a sealed flask. The solution was filtered and washed with dichloromethane (2×10 mL). The filtrate was then placed directly onto a 120 g-silica cartridge and was purified using eluent 10-70% MeOH/DCM. After evaporation, the product was isolated as a white foam (1.00 g), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710224B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-96b2d6ecc74443ad8ec9e7a7cf682d34 |
| Source note | uspto-grants-2014_04 |