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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 5-{4-[2(R)-t-butoxycarbonylaminopropoxy]benzyl}-3-triphenylmethylthiazolidine-2,4-dione | HCID 22854985 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-{4-[2(R)-Aminopropoxy]benzyl}thiazolidine-2,4-dione trifluoroacetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436257 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-a4868126da2d447fa02f5d34d8b71c39 |
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| Source note | uspto-grants-1995_07 |
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