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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium ChlorideHCID 5234—
ReactantEthylene carbonateHCID 7303—
Reactant1,3-DifluorobenzeneHCID 9741—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant1-(Ethoxycarbonyloxy)ethyl salicylateHCID 53826080—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetic AcidHCID 176—
Product1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylateHCID 13491395—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542158
Source datasetuspto-grants-1985_09
ORD IDord-ea78099213ba4e3993de00f16675cdd1
Source noteuspto-grants-1985_09