HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzoic Acid → Dibenzyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Benzyl 4-Hydroxybenzoate | HCID 7180 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Dibenzyl ether | HCID 7657 | — |
Reaction Steps
In the same way as in Example 13, 69.1 g (0.5 mole) of p-hydroxybenzoic acid and 216.2 g (2 moles) of benzyl alcohol were reacted at 120° C. for 4 hours in 138 g of toluene in the presence of 1.44 g of p-toluenesulfonic acid as a catalyst. The yield of benzyl p-hydroxybenzoate was 26%. Dimerization and dehydration of benzyl alcohol occurred simultaneously, and dibenzyl ether was formed in a ratio of as high as 45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973737 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-5520158b21af4788bd3bb3fd3af0fcf6 |
| Source note | uspto-grants-1990_11 |