HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359985Generated: October 30, 2026
Trifluoroacetic anhydride → HCID 67223534, compound
https://huagongshe.com/reaction/2359985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 4-[2-(2-Carbamoyl-ethyl)-5-phenylpyrrol-1-yl]-benzoic acid tert-butyl ester | HCID 67203231 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67223534 | HCID 67223534 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686015B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e0b53c4dc61843a7825b32151770ffba |
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| Source note | uspto-grants-2014_04 |
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