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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944447Generated: October 31, 2026

Trifluoroacetic acid → HCID 67044191, compound

https://huagongshe.com/reaction/1944447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantMethyl 2-(5-fluoro-2-methyl-1H-indol-1-yl)acetateHCID 58247161—
ReactantHCID 86652196HCID 86652196—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductHCID 67044191HCID 6704419171.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of triethylsilane (0.76 mL), trifluoroacetic acid (0.61 mL) and 1,2-dichloroethane (3.0 mL) at −10° C. was treated dropwise with a mixture of (5-fluoro-2-methylindol-1-yl)acetic acid methyl ester (0.070 g), 2-(2-chlorobenzenesulfonyl)-pyridine-3-carbaldehyde (0.089 g) and 1,2-dichloroethane (6.0 mL), and the resulting mixture was stirred at −10° C. for 15 minutes and then at room temperature for 4 hours. The mixture was diluted with dichloromethane, washed with saturated aqueous sodium hydrogen carbonate solution and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of ethyl acetate and pentane (1:4 to 4:1 by volume). Further purification by crystallisation from ethyl acetate and pentane gave the title compound as a white solid (0.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394836B2
Source datasetuspto-grants-2013_03
ORD IDord-0149da9f719b48cb978d0f0432585d9a
Source noteuspto-grants-2013_03