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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719730Generated: November 2, 2026

1-Chloroethyl 5-(2,4-difluorophenyl)salicylate → 1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate

https://huagongshe.com/reaction/1719730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl 5-(2,4-difluorophenyl)salicylateHCID 20266758—
ReactantSodium ethyl carbonateHCID 23677505—
SolventDimethylformamideHCID 6228—
Product1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylateHCID 13491395—

Reaction Steps

To a solution of 1-chloroethyl 5-(2,4-difluorophenyl)salicylate (5.0 g) in about 40 ml of DMF is added portionwise 3.0 g of sodium ethyl carbonate. The reaction is stirred at room temperature and then concentrated in vacuo. The concentrate is partitioned between ether/ethyl acetate and acidified water. The organic layer is separated and the aqueous layer is again extracted with ether, the organic layers are pooled and washed with water followed by drying and concentration to the crude product. After further purification by chromatography as described in Example 1, the product is crystallized from hexane to afford 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-2e181670a9584618adce48a18302962e
Source noteuspto-grants-1985_09