Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | L-Glutamine | HCID 5961 | — |
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (S)-N-tert-butylcarbonylalanine | HCID 42254381 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | L-Alanyl-L-Glutamine | HCID 123935 | 40% |
Reaction Steps
In a round bottom flask, add in 10 mmol of tert-butylcarbonylalanine (Boc-Ala), 15 mmol of triphenyl phosphine and 20 mmol of hexachloroethane, and then add in 20 ml of 1,2-dichloroethane. After reacting at 10° C. for 20 min, drop it into a liquid mixture containing 30 mmol glutamine, 20 ml of water and 20 ml of cyclohexane. While reacting, regulate pH to 11 with potassium hydroxide, the reaction temperature is 20° C., the reaction time after dropping is 30 min. And then acidify it to regulate pH=1.5 with dilute nitric acid. The aqueous phase, after concentrated, reacts with trifluoroacetic acid at room temperature for 15 hours. As the reaction is finished, add in 50 ml of ether, solids deposit, the product L-Ala-L-Gln with a yield of 40% is obtained by recrystallizing the solids with tetrahydrofuran-water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163917B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-fd5f25d28fb44971983842af9cd27cd5 |
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| Source note | uspto-grants-2007_01 |
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