HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356239Generated: October 28, 2026
Trifluoroacetic acid → HCID 15435851, compound
https://huagongshe.com/reaction/356239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 23298282 | HCID 23298282 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15435851 | HCID 15435851 | 22.7% |
Reaction Steps
A mixture of 3.55 g of 5-[4-(1-t-butoxycarbonyl-indolin-2-ylmethoxy)benzyl]-3-triphenylmethylthiazolidine-2,4-dione (prepared as described in Preparation 4) and 30 ml of trifluoroacetic acid was stirred at room temperature for 1 hour. At the end of this time, the reaction mixture was poured into water and the aqueous mixture was neutralized by the addition of sodium hydrogencarbonate, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography through silica gel, using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.41 g of the title compound. This product was dissolved in ethanol and precipitated by adding water, to give a powder melting at 55.8°-58.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834501 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-e55a92ac805d4c41a25ebb45d70e2500 |
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| Source note | uspto-grants-1998_11 |
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