HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 72085102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Bromothiophene-2-carbaldehyde | HCID 87792 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 72085102 | HCID 72085102 | 87.2% |
Reaction Steps
To a mixture of 4-bromothiophene-2-carboxaldehyde (1.91 g, 10.0 mmol) and 2,4-thiazolidinedione (1.40 g, 12.0 mmol) in ethanol (30 mL) was added piperidine (1.0 mL, 10.0 mmol). The reaction mixture was heated at reflux for 3 h, then cooled on an ice-bath, and the precipitated products were collected by filtration. The cake was washed with 40% ethanol and dried to afford 5-(4-bromothiophen-2-ylmethylene)-2,4-thiazolidinedione (2.53 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06452014B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-f1fa282738b840ddb40b25a4c4d9872a |
| Source note | uspto-grants-2002_09 |