HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719728Generated: November 1, 2026
Oxygen → 1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate
https://huagongshe.com/reaction/1719728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | 1,3-Difluorobenzene | HCID 9741 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(Ethoxycarbonyloxy)ethyl salicylate | HCID 53826080 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate | HCID 13491395 | — |
Reaction Steps
A glass-lined autoclave is charged with 1 mmole of palladium acetate, 5 mmole of sodium chloride, 1.6 mmole of sodium acetate, 2 mmole of phosphomolybdenovanadic acid, 10 g of ethylene carbonate, 5.0 ml of acetic acid, 465 mmole of 1-(ethoxycarbonyloxy)ethyl salicylate, and 510 mmole of m-difluorobenzene. The mixture is stirred for 48 hours at 90° C. and under 200 psi oxygen pressure. The solution is cooled to 25° C. and excess m-difluorobenzene is removed by distillation. Fifty ml of water and 150 ml of toluene are then added to the residue. The pH is adjusted to 7-8 with aqueous sodium hydroxide (80 mmoles). The layers are separated and the aqueous solution is extracted with 150 ml of toluene. The toluene and then the excess starting materials are removed by distillation. The resulting residue is recrystallized from methanol to obtain pure 1-(ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04542158 |
|---|
| Source dataset | uspto-grants-1985_09 |
|---|
| ORD ID | ord-ea78099213ba4e3993de00f16675cdd1 |
|---|
| Source note | uspto-grants-1985_09 |
|---|