HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Dibenzyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Dibenzyl ether | HCID 7657 | — |
Reaction Steps
When direct esterification was carried out using p-toluenesulfonic acid as a catalyst, the yield of the final product was very low. Even when toluene was used as an azeotropic dehydrating solvent, the yield was as low as 26%. In addition, under the reaction conditions employed, a greater portion of the charged benzyl alcohol self-condensed to form dibenzyl ether. The results are summarizd in Table 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973737 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-1c0ada15957a4051a8ccb1b5674d6655 |
| Source note | uspto-grants-1990_11 |