HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 4-Benzoyloxy-2-methylnaphthol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Menadiol | HCID 10209 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Benzoyloxy-2-methylnaphthol | HCID 22625409 | 69.3% |
Reaction Steps
9.7 g (0.056 mol) of 2-methyl-1,4-dihydroxynaphthalene was dissolved in 60 ml of pyridine, and, while stirring under ice-cooling, 8.4 g (0.06 mol) of benzoyl chloride was added dropwise. Following completion of the addition, stirring was continued under ice-cooling for 30 minutes, and for further one hour at room temperature. The reaction mixture was concentrated under reduced pressure, the residual oil extracted with ethyl acetate, washed with 1N HCl and then water, and the organic layer concentrated under reduced pressure. Methanol was added to the residue, the precipitated crystals collected by filtration and recrystallized from methanol to give 10.8 g of white crystals, m.p. 172-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358515B2 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-91770afe4a5f4c058ae10ae9f130275c |
| Source note | uspto-grants-2002_03 |