Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474295Generated: November 2, 2026

Hydrogen Peroxide → 5-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrile

https://huagongshe.com/reaction/1474295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant5-fluoro-1-methylidene-2,3-dihydro-1H-indene-4-carbonitrileHCID 68432012—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrileHCID 66646390—

Reaction Steps

5-Fluoro-1-methylidene-2,3-dihydro-1H-indene-4-carbonitrile (100 mg, 0.577 mmol) in THF (6 mL) at 0° C. was treated with borane tetrahydrofuran (1 M, 0.751 ml, 0.751 mmol). The resulting mixture was stirred for overnight at room temperature; LC analysis indicated consumption of starting material. To the mixture was added a combination of hydrogen peroxide (0.083 ml, 0.81 mmol) and 2M NaOH (0.404 ml, 0.808 mmol). The resulting mixture was then stirred for 2 hours. LC analysis indicated completion of the reaction. The reaction mixture was diluted with EtOAc, washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was absorbed into silica gel and loaded into silica column for separation with the solvent systems of hexanes/EtOAc (1/1) to give the desired product 5-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-8b68000398234cd59790f8645b2e2953
Source noteuspto-grants-2015_04