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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464691Generated: October 30, 2026

Water → HCID 53666165, compound

https://huagongshe.com/reaction/464691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86740378HCID 86740378—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 53666165HCID 5366616575.7%

Reaction Steps

1.44 g (0.06 mol) of sodium hydride (30% strength in paraffin oil) are added to a solution of 14.94 g (0.045 mol) of 3,3-dimethyl-2-[4-(1-hydroximinoethyl)-phenoxymethyl]-1-(1,2,4-triazol-1-yl)-2-butanol (Example 2) in 120 ml of absolute dimethylsulphoxide. The reaction mixture is stirred at room temperature for about 1 hour, until a clear solution has formed. 3.33 ml (0.06 mol) of 2,4-dichlorobenzyl chloride are then added and the reaction mixture is subsequently stirred at room temperature for 1.5 hours. Thereafter, water and glacial acetic acid are carefully added and the mixture is concentrated. The residue is taken up in ethyl acetate and the mixture is washed several times with dilute sodium chloride solution, dried over sodium sulphate and concentrated. The residue is chromatographed over a silica gel column (methylene chloride/ethyl acetate=4:1) and the product is recrystallized from acetonitrile. 16.2 g (73% of theory) of 2-{4-[1-(2,4-dichlorobenzylimino)-ethyl]-phenoxymethyl} -3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanol of melting point 101° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548945
Source datasetuspto-grants-1985_10
ORD IDord-cd5c287b14554451b9094849f19688fd
Source noteuspto-grants-1985_10