HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860556Generated: October 29, 2026
Toluene → 6-[3-(t-Butyl)-4-methoxyphenyl]-naphthalen-2-yl-methylene-2,4-thiazolidinedione
https://huagongshe.com/reaction/860556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 6-[3-(t-Butyl)-4-methoxyphenyl]-2-naphthaldehyde | HCID 86586043 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-[3-(t-Butyl)-4-methoxyphenyl]-naphthalen-2-yl-methylene-2,4-thiazolidinedione | HCID 86586042 | 28% |
Reaction Steps
A solution of toluene (2.5 mL), piperidine (0.003 mL), acetic acid (0.003 mL), 6-[3-(t-butyl)-4-methoxyphenyl]-2-naphthaldehyde (0.124 g, 0.31 mmol) and 2,4-thiazolidinedione (0.036 mg, 0.31 mmol) was heated at reflux for 16.5 hours under an argon atmosphere. The resulting suspension was filtered and the solid was stirred at room temperature in EtOH. After 3 hours, the solid was filtered and dried under high vacuum to afford 0.037 g (28%) of 6-[3-(t-butyl)-4-methoxyphenyl]-naphthalen-2-yl-methylene-2,4-thiazolidinedione, mp 274–276° C. 1H NMR (300 MHz, DMSO-d6): δ 1.40 (s, 9H), 3.86 (s, 3H), 7.11 (d, J=8.4 Hz, 1H), 7.63 (s, 1H), 7.66 (t, J=8.1 Hz, 2H), 7.88 (d, J=8.4 Hz, 1H), 7.92 (s, 1H), 8.07 (d, J=8.4 Hz, 1H), 8.08 (d, J=8.4 Hz, 1H), 8.17 (brs, 2H), 12.60 (brs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07153875B2 |
|---|
| Source dataset | uspto-grants-2006_12 |
|---|
| ORD ID | ord-245b17a7f23f4ecc8a67d40c045f6145 |
|---|
| Source note | uspto-grants-2006_12 |
|---|