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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165534Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 23042861, compound

https://huagongshe.com/reaction/2165534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 23042866HCID 23042866—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23042861HCID 23042861—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic anhydride (19.5 g) was added dropwise to a cooled (0° C.), stirred solution of 1-cyclopropylmethyl-1H-indole-3-carboxamide (5 g) in dioxane (100 ml) and triethylamine (18 g). After the addition the mixture was stirred at room temperature for two hours, the mixture was diluted with dichloromethane (200 ml) and washed with water (3×100 ml), dried (Na2SO4) and evaporated at reduced pressure. The residue was purified by column chromatography on silica eluting with dichloromethane to afford a colourless oil, (5 g); δH (CDCl3, 60 MHz) 0.3-0.6 (4H, m, 2×CH2), 0.9 (1H, m, CH), 4.0 (2H, d, J=7, CH2), 7.0-7.7 (5H, m); νmax 2210 (C≡N).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04940703
Source datasetuspto-grants-1990_07
ORD IDord-a5bfe6528b3a4da6ab47f3259ad09f82
Source noteuspto-grants-1990_07