HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-Methoxy-2-naphthaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxy-2-naphthaldehyde | HCID 76991 | — |
Reaction Steps
To a reactor equipped with a stirrer are charged 10 grams of 2-bromo-6-methoxynaphthalene prepared as in Example 7 hereof, 1.05 grams of magnesium and 35 mL of tetrahydrofuran (THF). The reaction is initiated by addition of a crystal of iodine. After one hour of heating at reflux with stirring, 10 mL of DMF mixed with 10 mL of THF is added and the mixture is again refluxed with stirring for 1.5 hours. The reaction mixture is hydrolyzed by addition of dilute acetic acid and a precipitate of crude 6-methoxy-2-naphthaldehyde is formed. The precipitate is recovered by filtration, washed with water, and purified by crystallization from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05907069 |
| Source dataset | uspto-grants-1999_05 |
| ORD ID | ord-dcdd0f716b5146b388df8cc2fe2fd992 |
| Source note | uspto-grants-1999_05 |