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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058501Generated: November 1, 2026

Trifluoroacetic acid → 4-Chloroindoline

https://huagongshe.com/reaction/2058501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Chloro-1,3-dihydro-2H-indol-2-oneHCID 1480686—
ReactantSodium borohydrideHCID 4311764—
Solvent1,4-DioxaneHCID 31275—
Product4-ChloroindolineHCID 301630677.4%

Reaction Steps

5.5 g of 4-chlorooxindole was dissolved in 80 ml of dioxane and 6.2 g of sodium borohydride was suspended in the resulting solution. 12.7 ml of trifluoroacetic acid (d=1.48) was added thereto dropwise at room temperature while stirring. After heat-refluxing the mixture for 4.5 hours, the solvent was removed therefrom under reduced pressure. Water was added to the residue and the water-insoluble materials were removed by filtration and washed with diethyl ether. The filtrate was extracted with diethyl ether and the ether layer was dried over anhydrous sodium sulfate followed by removing the solvent. The residue was distilled under reduced pressure to obtain 3.9 g of 4-chloroindoline as a colorless oily product having a boiling point of 135° C. at 10 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04317820
Source datasetuspto-grants-1982_03
ORD IDord-bc4193a30f9d4a839d2741e4bf1c6c0b
Source noteuspto-grants-1982_03