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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929287Generated: November 1, 2026

1-[2-Chloro-4-(4-chlorophenoxy)phenyl]-2-(1H-1,2,4-triazol-1-yl)ethanone → HCID 71258903, compound

https://huagongshe.com/reaction/929287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-Chloro-4-(4-chlorophenoxy)phenyl]-2-(1H-1,2,4-triazol-1-yl)ethanoneHCID 15753778—
ReactantHCID 178418918HCID 178418918—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71258903HCID 71258903—

Reaction Steps

The above-mentioned ethanone (120.0 g, 0.34 mol) was added to a solution of MgBr diethyl etherate (195.8 g, 0.76 mol) in dichloromethane (DCM, 2.5 L) and the mixture stirred at room temperature for about 90 min. This mixture was then cooled to about 0° C. and isopropyl magnesium chloride (344.5 mL of a 2 M solution in THF, 0.69 mol) was added dropwise. The mixture was allowed to warm to room temperature and was then quenched by addition of a saturated ammonium chloride solution. The organic components were extracted three times with DCM, the organic phases combined, dried and the solvents evaporated. Addition of MTBE resulted in precipitation of the unreacted starting material, which was filtered off. The filtrate was then purified using reverse phase chromatography to give 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol as a brown oil (31.1 g, 23%, HPLC Rt=1.305 min, masse=392).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09295259B2
Source datasetuspto-grants-2016_03
ORD IDord-70a5c9b0cf3c4997aa2df3c90f34cd10
Source noteuspto-grants-2016_03