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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721928Generated: October 31, 2026

alpha-(1-Ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-ethoxycarbonylmethoxybenzylalcohol → HCID 14622775, compound

https://huagongshe.com/reaction/1721928

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-(1-Ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-ethoxycarbonylmethoxybenzylalcoholHCID 20030167—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductHCID 14622775HCID 1462277591.8%

Reaction Steps

770 mg of α-(1-ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-ethoxycarbonylmethoxybenzylalcohol and 1.66 g of manganese dioxide are suspended in 30 ml of methylene chloride, and the suspension is stirred at room temperature for 24 hours. The reaction mixture is filtered and the filtrate is evaporated to remove solvent. The residue is triturated with a mixture of isopropyl ether and hexane to give 703 mg of ethyl [2,3-dichloro-4-(1-ethoxymethyl-5-pyrazolylcarbonyl)phenoxy]acetate as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853404
Source datasetuspto-grants-1989_08
ORD IDord-23b98d0e30544857bf6ad14b79aa5454
Source noteuspto-grants-1989_08