HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → L-Alanyl-L-Glutamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Glutamine | HCID 5961 | — |
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-carbobenzyloxyalanine | HCID 736104 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | L-Alanyl-L-Glutamine | HCID 123935 | 48% |
Reaction Steps
In a round bottom flask, add in 10 mmol each of carbobenzoxy-alanine (Z-Ala), triphenylphosphine and hexachloroethane respectively, and then 30 ml of toluene. After reacting at 0° C. for 3 h., drop it into a liquid mixture containing 25 mmol of glutamine and 20 ml of water. While reacting, regulate pH to 12 with sodium hydroxide, the reaction temperature is 15° C., the reaction time after dropping is 1.5 hours. And then acidify it to pH=2.5 with dilute hydrochloric acid. The aqueous phase, after concentrated, reacts with hydrogen gas in methanol at room temperature for 15 hours. The product L-Ala-L-Gln with a yield of 48% is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07163917B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-6643d91c744341a587477ff19123b0ca |
| Source note | uspto-grants-2007_01 |