Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | P-Cresol | HCID 2879 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | p-Cresol benzoate | HCID 11962 | 92% |
Reaction Steps
A mixture of 65.0 g (0.60 mol) of p-cresol, 92.7 g (0.66 mol) of benzoyl chloride, and 6 mL of anhydrous pyridine was refluxed for 1.5 hr and then added to 600 mL of 2% hydrochloric acid. The product was extracted with 2×100 mL of ether, the combined extract was washed by 2% NaOH, then dried over Na2SO4, and evaporated to dryness. Drying the residue in vacuum gave 117 g (92%) of p-tolyl benzoate (bp 127-135° C./25 mm Hg). A mixture of 117 g (0.552 mol) of p-tolyl benzoate and 92.0 (0.689 mol) of AlCl3 was slowly (for ca. 0.5 hr) heated to 120-125° C. This mixture was stirred at this temperature for 1 hr, and then 1000 mL of 2M HCl was added at 0° C. The product was extracted with 3×200 mL of diethyl ether, the combined extract was dried over Na2SO4 and then evaporated to dryness. This procedure gave 116 g (99%) of the title product which was further used without an additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08557936B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-68d049dc6f5347d99d64c7249c5a2995 |
|---|
| Source note | uspto-grants-2013_10 |
|---|