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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659934Generated: October 29, 2026

Sodium Iodide → ethyl 2,4-dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoate

https://huagongshe.com/reaction/659934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-(2-bromoethoxy)-2,4-dichlorobenzoateHCID 15029235—
ReactantHCID 178418441HCID 178418441—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl 2,4-dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoateHCID 57437285—
Productethyl 2,4-dichloro-3-[2-(1H-tetrazol-2-yl)ethoxy]benzoateHCID 66734875—

Reaction Conditions

Temperature80 °C

Reaction Steps

1H-tetrazol (0.45 g) and ethyl 3-(2-bromoethoxy)-2,4-dichlorobenzoate (2.00 g) were suspended in DMF (15 ml), potassium carbonate (1.21 g) and sodium iodide (0.04 g) were added thereto and the mixture was stirred at 80° C. for 3 hours. After the reaction, cool water was added, extracted with ethyl acetate (100 ml) and dried over anhydrous magnesium sulfate. The residue obtained by distilling off ethyl acetate was purified with silica gel column chromatography (elution solvent; ethyl acetate: hexane=1:1) to obtain the desired ethyl 2,4-dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoate (0.88 g) and ethyl 2,4-dichloro-3-[2-(1H-tetrazol-2-yl)ethoxy]benzoate (0.99 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084398B2
Source datasetuspto-grants-2011_12
ORD IDord-21b447b0c93749c0a26ac60350a7749f
Source noteuspto-grants-2011_12