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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992339Generated: October 29, 2026

1-(2,2,2-Trifluoroacetyl)indoline-5-carbonitrile → 2,3-Dihydro-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/1992339

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,2,2-Trifluoroacetyl)indoline-5-carbonitrileHCID 86625991—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product2,3-Dihydro-1H-indole-5-carbonitrileHCID 21907639—

Reaction Steps

1-(2,2,2-Trifluoroacetyl)-2,3-dihydro-1H-indole-5-carbonitrile (13 g, 0.0542 mol; see step (iii) above) was dissolved in THF (100 mL), to which 1% NaOH was then added. After stirring for 5 h at RT, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulfate and solvent was evaporated to provide the sub-title compound as a pale yellow solid. Yield: 8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648985B2
Source datasetuspto-grants-2010_01
ORD IDord-e04994d0e22040cdb6fb2c903fb41bd7
Source noteuspto-grants-2010_01