Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Aspartic Acid | HCID 5960 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Succinyl chloride | HCID 10970 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68650419 | HCID 68650419 | — |
Reaction Steps
This example that demonstrates how this method could be performed. 9.4 g aspartic acid, 10 ml triethyl amine and 100 ml tetrahydrofuran are transferred into a 100 ml flask fitted with a condenser and nitrogen inlet. The mixture is cooled to 0° C. and 5 g succinyl chloride is added and the mixture stirred under nitrogen atmosphere for 5 min and refluxed for 6 hours. The triethyl amine hydrochloride is filtered and the filtrate is concentrated by removing the solvent under vacuum. The residue is used directly for the subsequent reaction. The residue can be purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07597882B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-b9190018bb9a41e0888f68096d43b3c7 |
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| Source note | uspto-grants-2009_10 |
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