HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → o-Phenylene dibenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Water | HCID 962 | — |
| Product | o-Phenylene dibenzoate | HCID 69514 | 94% |
Reaction Steps
To 5.5 g pyrocatechol were added 50 ml tetrahydrofuran and 12.1 ml pyridine with stirring. Then to the resulting homogeneous mixture was slowly added 14.5 ml benzoyl chloride, and the reaction was stirred at room temperature for 1 hour, then heated refluxing for 4 hours. Next, 70 ml water was added to dissolve the resulting salt. The reaction mixture was extracted with toluene. Organic phase was separated, washed with saturated saline for two times, dried over anhydrous sodium sulfate. Removing solvent gave a white solid. After recrystallizing from ethyl acetate, 1,2-phenylene dibenzoate was obtained as a white crystal, the yield was 94%, and m.p. was 75-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07388061B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-0083c813f29248ca836499c60a0346a2 |
| Source note | uspto-grants-2008_06 |