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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089167Generated: October 25, 2026

Ammonium Chloride → alpha-(1-Methylpyrazol-5-yl)-2,3-dichloro-4,5-dimethoxybenzylalcohol

https://huagongshe.com/reaction/1089167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1H-Pyrazole, 1-methyl-HCID 70255—
Reactant2,3-Dichloro-4,5-dimethoxybenzaldehydeHCID 14748634—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productalpha-(1-Methylpyrazol-5-yl)-2,3-dichloro-4,5-dimethoxybenzylalcoholHCID 1474863590.5%

Reaction Steps

18 ml of 1.6M n-butyl lithium in n-hexane is added dropwise to a solution of 2.26 g of 1-methyl-pyrazole in tetrahydrofuran at -60° C. under argon gas atmosphere and the mixture is stirred at the same temperature for 1 hour. A solution of 5.88 g of 2,3-dichloro-4,5-dimethoxybenzaldehyde in tetrahydrofuran is added dropwise to the mixture at -60° to -50° C. and the mixture is stirred at -50° C. to room temperature for 1 hour. An aqueous ammonium chloride solution is added to the reaction mixture and the mixture is concentrated to remove organic solvent. The residue is extracted with ethyl acetate, and the extract is washed, dried and evaporated to remove solvent. The residue is crystallized from isopropyl ether to give 7.18 g of α-(1-methylpyrazol-5-yl)-2,3-dichloro-4,5-dimethoxybenzylalcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04965282
Source datasetuspto-grants-1990_10
ORD IDord-06102864382144748159a39cb0e918f3
Source noteuspto-grants-1990_10