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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 5-fluoro-1-methylidene-2,3-dihydro-1H-indene-4-carbonitrile | HCID 68432012 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018211B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-8b68000398234cd59790f8645b2e2953 |
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| Source note | uspto-grants-2015_04 |
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