Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649178Generated: October 30, 2026

Hydrochloric Acid → 3,3-Bisfluoromethyl-1-(4-chlorophenoxy)-1-(imidazol-1-yl)-butan-2-ol

https://huagongshe.com/reaction/1649178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant3,3-Bisfluoromethyl-1-(4-chlorophenoxy)-1-(imidazol-1-yl)-butan-2-oneHCID 13019437—
SolventMethanolHCID 887—
Product3,3-Bisfluoromethyl-1-(4-chlorophenoxy)-1-(imidazol-1-yl)-butan-2-olHCID 1301943869.2%

Reaction Steps

31.9 g (0.097 mol) of 3,3-bisfluoromethyl-1-(4-chlorophenoxy)-1-(imidazol-1-yl)-butan-2-one were dissolved in 600 ml of methanol, and 5.45 g (0.14 mol) of sodium borohydride were added in portions at 0° to 5° C. The mixture was subsequently stirred for 15 hours, 15 ml of concentrated hydrochloric acid were added and the mixture was stirred at room temperature for 2 hours. Thereafter, the reaction mixture was stirred into 800 ml of aqueous, saturated sodium bicarbonate solution. It was extracted with 1,000 ml of methylene chloride and the organic phase was washed twice with 1,000 ml of water each time, dried over sodium sulphate and concentrated by distilling off the solvent in vacuo. The oil which remained was stirred with isopropyl ether. 22.2 g (67.5% of theory) of 3,3-bisfluoromethyl-1-(4-chlorophenoxy)-1-(imidazol-1-yl)-butan-2-ol of melting point 137° C. were obtained. ##STR77##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415586
Source datasetuspto-grants-1983_11
ORD IDord-991b89c3282a4cbbaacca3d3d2f14dee
Source noteuspto-grants-1983_11