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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951612Generated: October 26, 2026

Ethyl chloroformate → [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

https://huagongshe.com/reaction/1951612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BicarbonateHCID 516892—
Reactant[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amineHCID 49866033—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amineHCID 4451139980%

Reaction Steps

To a solution of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine (2 mmol) in chloroform was added ethylchloroformate (>10 equiv.) and NaHCO3 (>20 equiv.) and this solution was refluxed for 3 h. After that, chloroform was evaporated and ethyl acetate was added and then this organic layer was washed with water 3 times. It was dried over MgSO4, filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was dissolved in ethanol and potassium hydroxide (>20 equiv.) dissolved in water was added and refluxed for 3 days. After that, ethyl acetate and sat. NaHCO3 were added and the organic layer was extracted. It was dried over MgSO4, filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate and methanol: Yield 80%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404730B2
Source datasetuspto-grants-2013_03
ORD IDord-b95b39df6ccb4ba69913c0ef3b3a78e8
Source noteuspto-grants-2013_03