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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851129Generated: November 1, 2026

Hydrochloric Acid → 1-(4-Chlorophenoxy)-4-fluoro-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol

https://huagongshe.com/reaction/851129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Chlorophenoxy)-3,3-dimethyl-4-fluoro-1-(1,2,4-triazol-1-yl)-2-butanoneHCID 20502660—
SolventMethanolHCID 887—
Product1-(4-Chlorophenoxy)-4-fluoro-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-olHCID 2050266272.4%

Reaction Steps

55 g (0.176 mol) of 1-(4-chlorophenoxy)-4-fluoro-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one (Example 1) were dissolved in 250 ml of methanol, and 3 g (0.08 mol) of sodium borohydride were added in portions. The reaction solution was subsequently stirred for 1 hour and then adjusted to a pH value of 3 with concentrated hydrochloric acid. After distilling off the solvent in vacuo, water was added to the residue and the mixture was extracted by shaking with methylene chloride. The combined organic phases were dried over sodium sulphate and concentrated in vacuo. The residue was crystallized with petroleum ether. 40 g (72% of theory) of 1-(4-chlorophenoxy)-4-fluoro-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol of melting point 103°-112° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382944
Source datasetuspto-grants-1983_05
ORD IDord-efaebfe225de4762820ee618a8c2884d
Source noteuspto-grants-1983_05