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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268901Generated: October 31, 2026

Tetrabutylammonium Fluoride → 5-(2-hydroxy-1-phenyl-ethyl)-1H-indole-2-carbonitrile

https://huagongshe.com/reaction/268901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactantbenzenesulfonyl-5-[2-(tert-butyl-dimethyl-silanyloxy)-1-phenyl-ethyl]-1H-indole-2-carbonitrileHCID 59831791—
Product5-(2-hydroxy-1-phenyl-ethyl)-1H-indole-2-carbonitrileHCID 5983185478.8%

Reaction Steps

A solution of tetrabutylammonium fluoride (1.0 M in THF, 1.6 mL) was added to a solution of -benzenesulfonyl-5-[2-(tert-butyl-dimethyl-silanyloxy)-1-phenyl-ethyl]-1H-indole-2-carbonitrile (0.56 g, 1.055 mmol) and the resulting mixture was refluxed for several hours. The solvent was evaporated under reduced pressure and the residue was diluted with water and ethyl acetate. The organic layer was separated, washed with brine, dried over anhydrous sodium sulfate filtered and evaporated under reduced pressure. The crude residue was purified by flash chromatography (EtOAc/hexane, 35/65 to 50/50) to afford 218 mg (75% yield) of 5-(2-hydroxy-1-phenyl-ethyl)-1H-indole-2-carbonitrile CCLXX as a light yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446118B2
Source datasetuspto-grants-2008_11
ORD IDord-72e2e1e65a9b418cacaec62d2b91ccca
Source noteuspto-grants-2008_11