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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648445Generated: October 30, 2026

Trifluoroacetic acid → 5-{4-[2(R)-Aminopropoxy]benzyl}thiazolidine-2,4-dione trifluoroacetate

https://huagongshe.com/reaction/1648445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant5-{4-[2(R)-t-butoxycarbonylaminopropoxy]benzyl}-3-triphenylmethylthiazolidine-2,4-dioneHCID 22854985—
SolventDichloromethaneHCID 6344—
Product5-{4-[2(R)-Aminopropoxy]benzyl}thiazolidine-2,4-dione trifluoroacetateHCID 22854983—

Reaction Steps

500 ml of trifluoroacetic acid were added dropwise to a solution of 85.5 g of 5-{4-[2(R)-t-butoxycarbonylaminopropoxy]benzyl}-3-triphenylmethylthiazolidine-2,4-dione, [prepared as described in step (a), above] in 700 ml of methylene chloride, whilst ice-cooling, and the mixture was stirred at room temperature for 4 hours. At the end of this time, the reaction mixture was freed from methylene chloride and trifluoroacetic acid by distillation under reduced pressure. The residue was then triturated with a mixture of benzene and a small amount of ethyl acetate, and the crystals which precipitated were collected by filtration. These crystals were recrystallized from a mixture of methanol and ethyl acetate to give 36.9 g of the title compound melting at between 162° C. and 166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436257
Source datasetuspto-grants-1995_07
ORD IDord-a4868126da2d447fa02f5d34d8b71c39
Source noteuspto-grants-1995_07