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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289078Generated: October 30, 2026

Trifluoroacetic acid → HCID 178520673, compound

https://huagongshe.com/reaction/2289078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178452033HCID 178452033—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductHCID 178520673HCID 178520673—

Reaction Steps

To a solution of the compound (2.50 g), which had been obtained in (1), in anhydrous dichloromethane (25 ml), trifluoroacetic acid (15 ml) was added dropwise under ice cooling, followed by stirring at the same temperature for 15 minutes and at room temperature for 15 minutes. The reaction mixture was diluted with 1,2-dichioroethane and concentrated by evaporation under reduced pressure. The residue was washed successively with hexane and diethyl ether by decantation and then the solvent was distilled off, whereby crude (3S)-3-[4-[2,3,-di(4-nitrobenzyloxycarbonyl)guanidino]butanoylamino]pyrrolidine trifluoroacetate (2.55 g) was obtained. The product was provided for use in the subsequent reaction without isolation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090802
Source datasetuspto-grants-2000_07
ORD IDord-13893cf886cd44e28fbf0e16b8bb6ec2
Source noteuspto-grants-2000_07