HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile, (1-naphthylmethylene)- → 2-[(2-Methoxyphenyl)(1-naphthyl)methyl]malononitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile, (1-naphthylmethylene)- | HCID 18092 | — |
| Reactant | HCID 178489560 | HCID 178489560 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(2-Methoxyphenyl)(1-naphthyl)methyl]malononitrile | HCID 11716587 | — |
Reaction Steps
A flask was charged with (1-naphthalenylmethylene)-propanedinitrile (408 mg, 2 mmol) and 10 mL anhydrous tetrahydrofuran. To this stirred solution was added, at room temperature, 2-methoxy phenyl magnesium bromide (2.4 mL, 2.4 mmol, 1 M in tetrahydrofuran). The reaction was stirred 1.5 hours, after which it was quenched with 1 N hydrochloric acid and taken up in ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate, brine, dried over magnesium sulfate, filtered, and evaporated to dryness. Following purification on silica (20% ethyl acetate/hexanes) 551 mg product was isolated as an off white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425580B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-b2ea1113d63c49478e6a3ed96726ce5a |
| Source note | uspto-grants-2008_09 |