HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-Benzyl-5-benzylidene-2-sulfanylidene-1,3-thiazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 3-(Phenylmethyl)-2-thioxo-4-thiazolidinone | HCID 97673 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Benzyl-5-benzylidene-2-sulfanylidene-1,3-thiazolidin-4-one | HCID 211635 | — |
Reaction Steps
A mixture of 3-benzylrhodanine (0.50 g, 2.2 mmol), benzaldehyde (0.23 mL, 2.3 mmol) and TEA (0.68 mL, 4.9 mmol) in MeCN (5 mL, anhyd) was heated at reflux. After 2 h the reaction mixture was cooled. Precipitated solids were collected by filtration, triturated with MeCN-Hex and dried under vacuum to yield 3-benzyl-5-benzylidene-2-thioxothiazolidin-4-one, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902237B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-6375490ab34540f08e3287c6fc1faa34 |
| Source note | uspto-grants-2011_03 |