HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthalenecarboxaldehyde → HCID 4045491, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| Reactant | 3,4-Dimethoxybenzeneacetonitrile | HCID 66727 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 4045491 | HCID 4045491 | 82.5% |
Reaction Steps
A mixture of 3,4-dimethyoxyphenylacetonitrile (1.77 g, 10.0 mmol, purchased from Tokyo Kasei,) and 2-naphthoaldehyde (1.56 g, 10.0 mmol, purchased from Tokyo Kasei) in 30 ml of ethanol was heated to dissolve. Two drops of 20% aqueous sodium hydroxide solution was then added and the reaction mixture was stirred over night. The precipitate was collected and washed with ethanol then with hexane, and dried to give 2.60 g (yield: 82.5%) of α-(3,4-dimethoxyphenyl-β-(naphthalen-2-yl)acrylonitrile as a yellow crystalline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05589506 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-5217ec9e44c7448381f8b70ae8e3e17f |
| Source note | uspto-grants-1996_12 |