Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587831Generated: October 31, 2026

Hydrochloric Acid → HCID 86666614, compound

https://huagongshe.com/reaction/587831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantTert-Butyl nitriteHCID 10906—
ReactantHCID 50940482HCID 50940482—
SolventWaterHCID 962—
ProductHCID 86666614HCID 8666661464%

Reaction Conditions

Temperature65 °C

Reaction Steps

N,N-dimethylformamide (3 ml) was heated to 65° C. and added with tert-butyl nitrite (0.15 g). To the solution, an N,N-dimethylformamide solution (2 ml) in which 3-amino-N-[2-ethyl-4-(1,1,1,2,3, 3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl) benzamide (0.5 g) has been dissolved was slowly added dropwise, while maintaining the temperature of 65° C. After confirming that no more gas is generated, the mixture was adjusted to room temperature and added with a mixture including 2N hydrochloric acid and a small amount of ice. The mixture was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with 2N hydrochloric acid, and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by column chromatography to obtain N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (0.31 g, yield 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227923B2
Source datasetuspto-grants-2016_01
ORD IDord-8d9eef45e2af4105b0ccf84c4e15c900
Source noteuspto-grants-2016_01