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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359985Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 67223534, compound

https://huagongshe.com/reaction/2359985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant4-[2-(2-Carbamoyl-ethyl)-5-phenylpyrrol-1-yl]-benzoic acid tert-butyl esterHCID 67203231—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67223534HCID 6722353462%

Reaction Steps

A stirred solution of 4-[2-(2-carbamoyl-ethyl)-5-phenylpyrrol-1-yl]-benzoic acid tert-butyl ester (3.92 mmol, 1.0 eq.) in dioxane and pyridine was cooled in an ice bath. To the mixture was added Trifluoroacetic anhydride (TFA, 7.84 mmol, 2.0 eq.). After 10 minutes the ice bath was removed and the reaction was allowed to warm to room temperature overnight. The solvent was evaporated in vacuo and the residue treated with EtOAc (250 mL) and saturated NaHCO3 (150 mL). The organic layer was separated, dried (Na2SO4) and the solvent evaporated in vacuo. The residue was loaded onto a 40 g RediSep silica-gel column for purification. Gradient elution with ethyl acetate/hexane (0% to 10% ethyl acetate in hexane over 25 minutes) gave the product as a yellow solid after combination of the appropriate fractions and evaporation of the solvent in vacuo, 62% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686015B2
Source datasetuspto-grants-2014_04
ORD IDord-e0b53c4dc61843a7825b32151770ffba
Source noteuspto-grants-2014_04