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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420593Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 18612732, compound

https://huagongshe.com/reaction/1420593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 18612733HCID 18612733—
SolventDichloromethaneHCID 6344—
ProductHCID 18612732HCID 18612732—

Reaction Steps

To a solution of 1.0 g (2.54 mmol) of methyl 3-hydroxy-2-{(4-methoxybenzenesulfonyl)-[2-(2,2,2-trifluoroacetylamino)benzyl]amino}propionate in 10 ml of CH2Cl2 was added 1.8 ml (12.7 mmol) of trifluoroacetic anhydride. After 1 hour at room temperature, the solvent was removed. Dichloromethane was added several times and the solvent removed under vacuum after each addition. Methanol was then added 2 times and the solvent removed under vacuum to give methyl 2-{(4-methoxybenzenesulfonyl)-[2-(2,2,2-trifluoroacetylamino)benzyl]-amino}acrylate as a glass. The glass was dissolved in methanol and 0.213 g of anhydrous NaHCO3 was added. The mixture was stirred at room temperature overnight and concentrated under vacuum to dryness. To the residue was added ethyl acetate and water. The organic layer was separated, washed with H2O, brine and dried with Na2SO4. The solvent was removed and the residue (1.0 g) was chromatographed on silica gel thick layer plates with hexane-ethyl acetate (1:1) as solvent to give 0.365 g of product as a glass. Anal. for C20H19F3N2O6S: Calc'd: C,50.9; H,4.1; N,5.9; F,12.1; S,6.7; Found: C,50.8; H,4.4; N,5.5; F,11.7; S,6.7; Mass spectrum (ES) 473.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071903
Source datasetuspto-grants-2000_06
ORD IDord-8e676e7d40114051848ef6b9334b1264
Source noteuspto-grants-2000_06