HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-(2-Carboxy-alpha-methylbenzylidene)rhodanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzoylacetic acid | HCID 97045 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Rhodanine | HCID 1201546 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Carboxy-alpha-methylbenzylidene)rhodanine | HCID 73793485 | — |
Reaction Steps
To a hot stirred solution of 2-carboxyacetophenone (1.91 g., 11.65 mM) and 1.57 g. (11.75 mM) of rhodanine in 8 ml. of acetic acid is added 3.12 g. (38.1 mM) of sodium acetate. The solution is refluxed for 3.5 hours, cooled, and poured into water, whereupon a gum forms. The gum crystallizes and is collected and recrystallized from methanol to give 5-(2-carboxy-α-methylbenzylidene) rhodanine as yellow-brown crystals, m.p. 193°-195°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018891 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-58087806d377466b9974f28fcd7f98da |
| Source note | uspto-grants-1977_04 |