HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydroquinone → 4-Benzoyloxy-2-methylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydroquinone | HCID 7253 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Product | 4-Benzoyloxy-2-methylphenol | HCID 14650330 | 68.2% |
Reaction Steps
Using 2.5 g of methylhydroquinone and 2.8 g of benzoyl chloride, the procedure in Reference Example was followed. Recrystallization from ethanol-isopropyl ether gave 3.1 g of 4-benzoyloxy-2-methylphenol as white crystals, m.p. 120-122° C. Then, using 2.3 g of the crystals, 1.4 g of anhydrous potassium carbonate, 4.6 g of chloromethyloxirane and 1.9 g of 1-(2-methoxyphenyl)piperazine, the procedures of Examples 3 and 4 were followed to give 3.2 g of white crystals, m.p. 192-194° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358515B2 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-1e798493ce78462eb830a138848a9708 |
| Source note | uspto-grants-2002_03 |