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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519326Generated: October 26, 2026

Trifluoroacetic anhydride → Ethyl 7-oxo-1,4,5,6-tetrahydroindole-2-carboxylate

https://huagongshe.com/reaction/519326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant4-(5-(Ethoxycarbonyl)-1H-pyrrol-3-yl)butanoic acidHCID 15272822—
SolventTrifluoroacetic acidHCID 6422—
ProductEthyl 7-oxo-1,4,5,6-tetrahydroindole-2-carboxylateHCID 84853287%

Reaction Steps

Into a 1000-mL round-bottom flask was placed a solution of 113h (30 g, 133.19 mmol, 1.00 equiv) in CF3COOH (500 mL) and trifluoroacetyl 2,2,2-trifluoroacetate (42 g, 199.97 mmol, 1.50 equiv). See FIG. 14. The resulting solution was stirred at room temperature for 60 min, concentrated under vacuum, diluted with 500 mL of water and 500 mL of EA, and extracted with 3×500 mL of ethyl acetate. The combined organic layers were washed with 1×500 mL of saturated aqueous potassium carbonate and 1×500 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum to afford 24 g (87%) of 113i as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115152B2
Source datasetuspto-grants-2015_08
ORD IDord-2f9f96070fea4ce2a30a50e760373e53
Source noteuspto-grants-2015_08