Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777356Generated: October 31, 2026

1-Hydroxybenzotriazole hydrate → 4-[5-(3-Chloro-4-cyclohexylphenyl)-1,2,4-oxadiazol-3-yl]benzenemethanol

https://huagongshe.com/reaction/1777356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-Chloro-4-cyclohexylbenzoic acidHCID 20310416—
ReactantHCID 178513316HCID 178513316—
SolventDimethylformamideHCID 6228—
Product4-[5-(3-Chloro-4-cyclohexylphenyl)-1,2,4-oxadiazol-3-yl]benzenemethanolHCID 70869456—

Reaction Conditions

Temperature132.5 °C

Reaction Steps

N,N-Dicyclohexylcarbodiimide (0.615 g, 0.003 mol) is added to a solution of 3-chloro-4-cyclohexyl benzoic acid (0.475 g, 0.002 mol), N-hydroxy-4-hydroxymethylbenzamidine (0.45 g, 0.003 mol) and N-hydroxybenzotriazole monohydrate (0.457 g, 0.003 mol) in N,N-dimethylformamide (10 mL). The reaction mixture is stirred at 130-135° C. for 2 hrs. It is then cooled to 0-5° C., filtered and washed with dichloromethane (2×20 mL). The filtrate is evaporated under reduced pressure and the residue is treated with demineralized water (20 mL). It is extracted with ethyl acetate (3×15 mL) and the combined extract is dried over sodium sulfate. Removal of solvent under reduced pressure gives a crude residue which is purified by column chromatography (silica gel 230-400, ethyl acetate:toluene, 15:85) to give {4-[5-(3-chloro-4-cyclohexylphenyl)-[1,2,4]-oxadiazol-3-yl]phenyl}methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266867B2
Source datasetuspto-grants-2016_02
ORD IDord-e34a51f808bb4e75ae0fc33c4daf3307
Source noteuspto-grants-2016_02