HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 8-(6-Formylnaphthalen-2-yloxy)octanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Bromooctanoic acid | HCID 548275 | — |
| Reactant | 6-Hydroxy-2-naphthaldehyde | HCID 2764110 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Naphtholate | HCID 12168161 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-(6-Formylnaphthalen-2-yloxy)octanoic acid | HCID 57457039 | 56.1% |
Reaction Steps
The intermediate aldehyde for this compound was prepared by a slightly modified procedure: 6-Hydroxynaphthalene-2-carbaldehyde (1.0 g, 5.8 mmol) was dissolved in DMF (10 mL) and sodium hydride 60% (278 mg) was added and the mixture stirred at RT for 15 min. 8-Bromooctanoic acid (0.37 g, 1.7 mmol) was converted to the sodium salt by addition of sodium hydride 60% and added to an aliquot (2.5 mL) of the above naphtholate solution and the resulting mixture was stirred at RT for 16 hours. Aqueous acetic acid (10%) was added and the mixture was extracted 3 times with diethyl ether. The combined organic phases were dried with MgSO4 and evaporated to dryness affording 300 mg of 8-(6-formylnaphthalen-2-yloxy)octanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879893B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-7160a50037724d7182b890bf5e632b28 |
| Source note | uspto-grants-2011_02 |