Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389125Generated: November 1, 2026

Methanol → HCID 86653015, compound

https://huagongshe.com/reaction/389125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58243475HCID 58243475—
CatalystCobalt(II) chlorideHCID 24288—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86653015HCID 8665301581.2%

Reaction Steps

Sodium borohydride (245 mg) was added to a mixture of 3-chloro-4-{4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzonitrile (438 mg), cobalt chloride (II) hexahydrate (515 mg) and methanol (10 ml), followed by stirring at room temperature for one hour. Water, a 1M aqueous sodium hydroxide solution and ethyl acetate were added to the reaction solution, followed by celite filtration. The filtrate was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:methanol=100:1 to 10:1). The resulting residue was dissolved in ethyl acetate, 4M hydrogen chloride-ethyl acetate (2 ml) was added thereto and the solvent was evaporated under reduced pressure. The residue was washed with ethyl acetate to obtain 1-(3-chloro-4-{4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}phenyl}methanamine dihydrochloride (141 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-f8ae5a284cbe4941a53f7553c8719182
Source noteuspto-grants-2013_02