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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102717Generated: November 2, 2026

Trifluoroacetic acid → HCID 57803073, compound

https://huagongshe.com/reaction/2102717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 57803055HCID 57803055—
SolventEthyl AcetateHCID 8857—
ProductHCID 57803073HCID 57803073—

Reaction Conditions

Temperature90 °C

Reaction Steps

Crude rac-6-chloro-3-hydroxy-3-naphthalen-2-yl-1,3-dihydro-indol-2-one (0.15 g, 0.48 mmol) (from Example 47a supra) was suspended in a mixture of triethylsilane (0.23 mL, 1.44 mmol) (Aldrich) and trifluoroacetic acid (0.83 g, 7.2 mmol) and heated in an 90° C. oil bath for 17 hours. After cooling to room temperature, mixture was diluted with ethyl acetate and treated with solid sodium carbonate (1 g). After stirring for 30 minutes, mixture was extracted with water and brine. Aqueous layers were back washed with ethyl acetate. Organic layers were combined, dried (MgSO4), filtered and concentrated. Residue was recrystallized from dichloromethane-hexanes to give rac-6-chloro-3-naphthalen-2-yl-1,3-dihydro-indol-2-one as brown solid. (Yield 0.08 g, 56%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-475f4d74d03b4d789729366061bc340b
Source noteuspto-grants-2009_08