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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033738Generated: October 30, 2026

Anisole → HCID 15264020, compound

https://huagongshe.com/reaction/1033738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantHCID 20079600HCID 20079600—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 15264020HCID 1526402086%

Reaction Conditions

Temperature70 °C

Reaction Steps

To 72.0 g (172 mmol) of (+)-2-(2,4-difluoro-phenyl)-3-((4-methoxyphenyl)methylthio)-3-methyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol were added 18.6 g (172 mmol) of anisole and 1010 ml of trifluoroacetic acid in this order, followed by stirring at 70° C. for 1.5 hours. After allowing the mixture to cool, the solvent was removed by distillation under reduced pressure, and the residue was neutralized with a saturated sodium hydrogencarbonate aqueous solution, followed by extraction with dichloromethane. The organic layer was washed with a saturated sodium chloride aqueous solution and dried. The solvent was removed by distillation under reduced pressure, and the residue was purified by column chromatography using chloroform as an eluent. The solvent was removed by distillation under reduced pressure, and the residue was recrystallized from a mixed solvent of isopropyl ether and hexane to obtain 44.1 g (86%) of (-)-2-(2,4-difluoro-phenyl)-3-mercapto-3-methyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312815
Source datasetuspto-grants-1994_05
ORD IDord-d57fa6bff5cf418e908a29e73dc5ffd6
Source noteuspto-grants-1994_05