HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482523Generated: October 31, 2026
Acetic Acid → 5-(4-Methoxycarbonylmethyloxybenzyl)thiazolidine-2,4-dione
https://huagongshe.com/reaction/482523
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 5-(4-Methoxycarbonylmethoxybenzyl)-3-triphenylmethylthiazolidine-2,4-dione | HCID 22119050 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(4-Methoxycarbonylmethyloxybenzyl)thiazolidine-2,4-dione | HCID 23514198 | 85.6% |
Reaction Steps
1700 ml of acetic acid and then 400 ml of water were added at room temperature to a suspension of 344 g of 5-(4-methoxycarbonylmethoxybenzyl)-3-triphenylmethyl-thiazolidine-2,4-dione [prepared as described in step (f) above] in 400 ml of 1,4-dioxane and the resulting mixture was stirred for 5 hours at 80° C. At the end of this time, the reaction mixture was freed from the solvent by evaporation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel using a 1:2 by volume mixture of ethyl acetate and hexane, a 2 1 by volume mixture of ethyl acetate and hexane and then ethyl acetate as eluents, to give 161.7 g of the title compound, melting at 100°-106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05798375 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-289cd1e97bde4fcf80154f258749095b |
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| Source note | uspto-grants-1998_08 |
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