HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55494Generated: October 29, 2026
Hydrochloric Acid → 5-[4-(2-Oxoethoxy)benzyl]thiazolidine-2,4-dione
https://huagongshe.com/reaction/55494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23298348 | HCID 23298348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[4-(2-Oxoethoxy)benzyl]thiazolidine-2,4-dione | HCID 10849277 | 75.2% |
Reaction Steps
20 ml of 6N aqueous hydrochloric acid were added to a solution of 10.07 g of 5-[4-(2,2-diethoxyethoxy)benzyl]thiazolidine-2,4-dione (prepared as described in Preparation 46) in 80 ml of tetrahydrofuran, and the resulting mixture was allowed to stand overnight at room temperature. At the end of this time, the reaction mixture was freed from the solvent by distillation under reduced pressure. The residue was diluted with water, after which it was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through silica gel, using a 2:3 by volume mixture of hexane and ethyl acetate as the eluent, to give 5.92 g of the title compound having Rf=0.37 (on silica gel thin layer chromatography using a 1:2 by volume mixture of hexane and ethyl acetate as the developing solvent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624935 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-22e01e3b4255462093a5229ae5a618fe |
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| Source note | uspto-grants-1997_04 |
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