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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719727Generated: November 2, 2026

Salicylic Acid → 1-(Ethoxycarbonyloxy)ethyl salicylate

https://huagongshe.com/reaction/1719727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylic AcidHCID 338—
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantCarbonic acid, 1-chloroethyl ethyl esterHCID 162095—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(Ethoxycarbonyloxy)ethyl salicylateHCID 53826080—

Reaction Steps

A mixture of 2.76 g salicylic acid, 2.02 g triethylamine and 3.5 gm 1-chloroethyl ethyl carbonate in 25 ml of toluene is refluxed for three hours. The reaction mixture is cooled and 25 ml of ether and 25 ml of water added. The organic layer is separated, washed 2× with 25 ml water, dried through sodium sulfate and concentrated in vacuo. The residue (3.88 g) is chromatographed on 200 g silica gel. Elution with 25% methylene chloride in hexane gives 1-(ethoxycarbonyloxy)ethyl salicylate which is directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542158
Source datasetuspto-grants-1985_09
ORD IDord-a70b2a22e28b40d7b4e2dc80c76ead48
Source noteuspto-grants-1985_09