HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → Benzyl (2S)-3-(2-bromophenyl)-2-{[(2R)-2-bromopropanoyl]amino}-propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2R)-2-bromopropionyl chloride | HCID 6997261 | — |
| Reactant | benzyl (S)-2-bromophenylalaninate | HCID 11716996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl (2S)-3-(2-bromophenyl)-2-{[(2R)-2-bromopropanoyl]amino}-propanoate | HCID 10367385 | — |
Reaction Steps
Introduce 25.7 g of benzyl (S)-2-bromophenylalaninate and 150 ml of dichloromethane into a reactor, then bring the temperature of the reaction mixture to 0° C. and add 20 ml of diisopropylethylamine followed by 13.2 g of (2R)-2-bromopropionyl chloride. Subsequently, bring the mixture to ambient temperature. After stirring for 1 hour at that temperature, wash the mixture with water and then with dilute acetic acid solution, and evaporate off the solvents to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208607B1 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-ea10b4f1cb964df7a4e21cd1dcd2feb1 |
| Source note | uspto-grants-2007_04 |