Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycylglycine | HCID 11163 | — |
| Product | HCID 21466888 | HCID 21466888 | — |
Reaction Steps
Into a 500-ml flask were placed 13.2 g of glycylglycine, 200 ml of methanol, 20 g of triethylamine, and 15 g of carbon disulfide. The contents were stirred at 30° C. for 1 hour. A solution of 12.3 g of ethyl chloroacetate in 50 ml of methanol was added thereto dropwise, and this mixture was stirred at room temperature for 30 minutes. The resulting solution assumed a yellowish orange color. After the solvent was distilled off under reduced pressure, 50 ml of ethanol was added to the residue, and a solution of 15 g of potassium acetate in 300 ml of ethanol was added thereto. The crystals precipitated were taken out by filtration and washed with ethanol to obtain 15.4 g of rhodanin-3-ylmethylcarbamoylacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665887 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-f6ce621ba46c4da7b62f799bebf71245 |
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| Source note | uspto-grants-1997_09 |
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