HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-(Benzyloxy)naphthalene-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Hydroxynaphthalene-2-carbonitrile | HCID 22243621 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-(Benzyloxy)naphthalene-2-carbonitrile | HCID 22243428 | 90.3% |
Reaction Steps
Sodium hydride (151 mg, 60% in mineral oil, 3.77 mmol) is added to a stirring solution of 7-hydroxy-2-naphthonitrile (530 mg, 3.14 mmol) in DMSO (10 mL). After the bubbling subsides, benzyl bromide (448 μL, 3.77 mmol) is added and the resulting mixture is allowed to stir for 4 hours. The reaction mixture is poured into water and extracted with ether. The ether layer is dried (Na2SO4), filtered, and concentrated to dryness. The product is purified by column chromatography (step gradient, 25 to 50% CH2Cl2 in hexanes) to give 7-benzyloxy-2-naphthonitrile (735 mg, 90%) as a white solid. HRMS (EI) calculated for C18H13NO: 259.0997, found 259.0993.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001900B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-312464c0cc5c458b901921ecf26e109d |
| Source note | uspto-grants-2006_02 |