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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356239Generated: October 28, 2026

Trifluoroacetic acid → HCID 15435851, compound

https://huagongshe.com/reaction/356239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23298282HCID 23298282—
SolventWaterHCID 962—
ProductHCID 15435851HCID 1543585122.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834501
Source datasetuspto-grants-1998_11
ORD IDord-e55a92ac805d4c41a25ebb45d70e2500
Source noteuspto-grants-1998_11