HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Oxo-2,3-Dihydro-1H-Indene-4-Carbonitrile → 1-hydroxy-2,3-dihydro-1H-indene-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Oxo-2,3-Dihydro-1H-Indene-4-Carbonitrile | HCID 2751583 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-hydroxy-2,3-dihydro-1H-indene-4-carbonitrile | HCID 14515307 | 82% |
Reaction Steps
To a stirring suspension of 1-oxo-2,3-dihydro-1H-indene-4-carbonitrile INT-45 (1.2 g, 7.64 mmol) and silica gel (catalytic) in EtOH at 0° C. was added NaBH4 (237.2 mg, 7.64 mmol). The reaction was allowed to warm to room temperature and stirred for 2 h. The solvent was removed under reduced pressure, and the product was purified by chromatography (EA/hexane) to afford 1.02 g (82%) of 1-hydroxy-2,3-dihydro-1H-indene-4-carbonitrile INT-46 as a white solid. LCMS-ESI (m/z) calculated for C10H9NO; 159.2; found 160.1 [M+H]+, tR=2.39 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357706B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-42c8c944c5ad46b1bcc2e0e8e9211944 |
| Source note | uspto-grants-2013_01 |