HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742505Generated: November 4, 2026
Hydrochloric Acid → 5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dione
https://huagongshe.com/reaction/1742505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 11027585 | HCID 11027585 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dione | HCID 2818126 | 83.2% |
Reaction Steps
A solution of 2.99 g of a 28% w/v methanolic solution of sodiumamethoxide in 10 ml of methanol was added dropwise, whilst ice-cooling, to a solution of 7.86 g of 5-(4-acetoxybenzyl)-3-triphenylmethyl-thiazolidine-2,4-dione [prepared as described in step (c) above] in 70 ml of toluene, and the resulting mixture was stirred at room temperature for 1 hour, after which it was allowed to stand overnight at the same temperature. The pH of the reaction mixture was then adjusted to a value of 4 by the addition of 1N aqueous hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the crystals which appeared in the residue were collected, washed with hexane and dried, to give 6.0 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05338855 |
|---|
| Source dataset | uspto-grants-1994_08 |
|---|
| ORD ID | ord-ebfbb6c80cd447a28787da56f35b864a |
|---|
| Source note | uspto-grants-1994_08 |
|---|