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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533196Generated: November 2, 2026

Iodoethane → (3,5-Dichloro-4-ethoxy-phenyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1533196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant(3,5-Dichloro-4-hydroxy-phenyl)-carbamic Acid Tert-butyl EsterHCID 22048528—
SolventAcetoneHCID 180—
Product(3,5-Dichloro-4-ethoxy-phenyl)-carbamic acid tert-butyl esterHCID 54404293—

Reaction Steps

To a solution of (3,5-dichloro-4-hydroxy-phenyl)-carbamic acid tert-butyl ester (1.0 g) and potassium carbonate (1.0 g) in acetone (18 mL) is added ethyl iodide (0.36 mL) and the mixture is stirred for approximately 15 hours at room temperature. The solution is then filtered, concentrated under reduced pressure, and partitioned between ethyl acetate and water. The separated aqueous layer is further extracted twice with ethyl acetate, and the pooled organic extracts are washed successively with 10% aqueous sodium hydroxide, with water, and then dried over anhydrous sodium sulfate. Evaporation of the solvent under reduced pressure gave the desired product as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207715B1
Source datasetuspto-grants-2001_03
ORD IDord-a087a64f2aa0462ea66a33275c1ad6f2
Source noteuspto-grants-2001_03