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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592010Generated: October 30, 2026

Trifluoroacetic acid → HCID 58997409, compound

https://huagongshe.com/reaction/1592010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67140081HCID 67140081—
SolventDichloromethaneHCID 6344—
ProductHCID 58997409HCID 58997409—

Reaction Steps

The title C compound, 4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-ylmethyl)-benzoic acid 4-t-butoxycarbonyl-benzyl ester (119 mg, 0.19 mmol) is dissolved in CH2Cl2 (5 mL) and then added TFA (5 mL, 64.9 mmol). This is stirred for 2 h and then concentrated under reduced pressure. The residue is suspended in MeCN:water (6:4) (12 mL), centrifuged, decanted and filtered through a 0.1 micron Acrodisc filter. The resulting mixture is loaded onto a preparative reverse phase HPLC column (YMC CombiPrep Pro C18, 50×20 mm I.D., particle size S-5 micron, 12 nM) in 6 aliquots and eluted at 30 mL/min with a gradient of 90:10 (water containing 0.1% TFA: MeCN) at 0 min to 10:90 at 5 min. Then held at 10:90 until 7 min. Fractions containing product are combined and concentrated by lyophilization to yield 4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-ylmethyl)-benzoic acid 4-carboxy-benzyl ester as a white amorphous solid: [M−1]−=403.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291635B2
Source datasetuspto-grants-2007_11
ORD IDord-7be1f1cc7cac4d3ca987eb298eef2b96
Source noteuspto-grants-2007_11