Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Rhodanine | HCID 1201546 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22007864 | HCID 22007864 | 78.3% |
Reaction Steps
In 150 mL of acetic acid, were suspended 11.7 g (121 mmol) of furfural and 16.25 g (122 mmol) of rhodanine. To the suspension, was added 31.0 g (378 mmol) of sodium acetate, and the mixture was stirred at 85° C. for 1 hour and 40 min. After confirming the appearance of a bright orange precipitate, the reaction suspension was cooled to room temperature and poured into 200 mL of water. After thorough stirring, the resulting precipitate was filtered under reduced pressure, and the residue was washed with 300 mL of water, 20 mL of 99.5% ethanol, and then 10 mL of diethyl ether. The residue was dried to give 20.0 g (94.8 mmol) of furfural rhodanine with a crude yield of 78%. The furfural rhodanine was used for the subsequent reaction without being further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06215016B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-305d2b3861b54134ba1f5454f76c26c3 |
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| Source note | uspto-grants-2001_04 |
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