HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-[(2,5-Bis-benzyloxyphenyl)methylene]-4-oxo-2-thioxo-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Rhodanine | HCID 1201546 | — |
| Reactant | 2,5-Bis(benzyloxy)benzaldehyde | HCID 3530399 | — |
| Reactant | Piperidine, acetate | HCID 9793820 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[(2,5-Bis-benzyloxyphenyl)methylene]-4-oxo-2-thioxo-thiazolidine | HCID 73455997 | — |
Reaction Steps
1.59 g (5 mmol) of 2,5-bis-benzyloxybenzaldehyde, 0.73 g (5.5 mmol) of rhodanine, 0.29 g (2 mmol) of piperidine acetate and 40 ml of toluene were heated on a water separator under a nitrogen atmosphere for 1.5 hours. After cooling, the yellow crystals were filtered off under suction, washed with toluene and diethyl ether and dried in a vacuum: 1.34 g (62%) of 5-[(2,5-bis-benzyloxyphenyl)methylene]-4-oxo-2-thioxo-thiazolidine; 1HNMR (DMSO-d6, 250 MHz) δ 13.80 (s, 1H), 7.80 (s, 1H), 6.85-7.50 (m, 13H), 5.19 (s, 2H), 5.10 (s, 2H); TLC (toluene/methyl ethyl ketone/glacial acetic acid (72:20:8)): Rf=0.80.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506755B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-71230f2f98ef4511a897c5213c856e18 |
| Source note | uspto-grants-2003_01 |