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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844557Generated: October 29, 2026

Hydrochloric Acid → 3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol

https://huagongshe.com/reaction/844557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-alHCID 22613804—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-olHCID 2261382985.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (0.52 g) was added in three portions, over 5 minutes, to an ice-cooled solution of 3-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-al (3.3 g) (see Preparation 18) in ethanol (25 ml). The mixture was stirred for a further hour before removing the solvent under reduced pressure to give a residue. The residue was then suspended in water (50 ml), cooled to 0° C. and the mixture first acidified to pH1 with 2N aqueous hydrochloric acid solution and then basified to pH14 by addition of solid sodium carbonate before being extracted with ethyl acetate (3×200 ml). The organic phases were combined, dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to yield 3-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol (2.84 g) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380396B1
Source datasetuspto-grants-2002_04
ORD IDord-c07ef107c544415682a02fa84242a7c6
Source noteuspto-grants-2002_04