HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(4-[2-(4-Tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | tert-butyl N-{4-[2-(4-formylphenoxy)ethyl]phenyl}carbamate | HCID 21704970 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(4-[2-(4-Tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione | HCID 54100550 | 72.6% |
Reaction Steps
A solution of 3.41 g (10 mmole) tert-butyl N-{4-[2-(4-formylphenoxy)ethyl]phenyl}carbamate and 1.29 g (11 mmole) 2,4-thiazolidinedione in toluene containing a catalytic amount of piperidinium acetate was refluxed in a Dean-Stark water trap for 3 hours. The reaction was followed by TLC and more 2,4-thiazolidinedione was added during the reaction time. The solution was cooled to room temperature filtered and the precipitate was refluxed in methanol. Another filtration gave 3.2 g (yield 72.6%) 5-(4-[2-(4-tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione as a light yellow, solid substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288096B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-d4ad7562dded438cb015b98b0f89d2f4 |
| Source note | uspto-grants-2001_09 |