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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291715Generated: November 2, 2026

4-Chlorophenol → HCID 13254745, compound

https://huagongshe.com/reaction/2291715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantSodiumHCID 5360545—
Reactant2-(Methoxy-tert.-butyl)-2-(1,2,4-triazol-1-yl-methyl)-oxiraneHCID 13254740—
SolventEthanolHCID 702—
ProductHCID 13254745HCID 1325474564.6%

Reaction Steps

8.1 g (0.0633 mol) of 4-chlorophenol were added to a solution of 0.32 g (0.014 mol) of sodium in 100 ml of absolute ethanol. 10.3 g (0.0488 mol) of 2-(methoxy-tert.-butyl)-2-(1,2,4-triazol-1-yl-methyl)-oxirane, dissolve in 300 ml of absolute ethanol, were added, and the reaction mixture was heated under reflux for 48 hours. The reaction mixture was allowed to cool and was concentrated. The residue was taken up in ethyl acetate, and the solution was washed once with water, once with 1N sodium hydroxide solution, again with water, thereafter with 1N hydrochloric acid and 1N sodium hydroxide solution, again with water, and finally with saturated sodium chloride solution. The organic phase was dried over sodium sulphate, and concentrated. 10.7 g (64.6% of theory) of 2-(4-chlorophenoxymethyl)-3,3-dimethyl-4-methoxy-1-(1,2,4-triazol-1-yl)-butan-2-ol of refractive index nD20 =1.531 were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797499
Source datasetuspto-grants-1989_01
ORD IDord-fe7ae77932944af1ba22b44353aafca2
Source noteuspto-grants-1989_01