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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126882Generated: October 30, 2026

Water → Triadimenol-tert-butylhydroxy

https://huagongshe.com/reaction/126882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Chlorophenoxy)-3-(hydroxymethyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-2-butanoneHCID 20288241—
SolventIsopropanolHCID 3776—
ProductTriadimenol-tert-butylhydroxyHCID 2028824968.2%

Reaction Steps

25 g (0.08 mol) of 1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-3,3-dimethyl-4-hydroxy-butan-2-one were dissolved in 350 ml of isopropanol, and 3.5 g of sodium borohydride were added in portions at room temperature. The mixture was stirred at room temperature for 15 hours, 500 ml of water were added, the mixture was stirred at room temperature for a further 15 hours, 300 ml of methylene chloride were added and the organic phase was washed three times with 100 ml of water each time. The organic phase was dried over sodium sulphate, the solvent was distilled off under a waterpump vacuum and 100 ml of ether were added to the residue. 17 g (67.6% of theory) of 1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-3,3-dimethyl-butane-2,4-diol were obtained as colorless crystals of melting point 110°-112° C. ##STR19##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254132
Source datasetuspto-grants-1981_03
ORD IDord-a3246066df934bcdb734d5e1ca7c885a
Source noteuspto-grants-1981_03