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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53663Generated: October 25, 2026

Sodium Hydroxide → Efinaconazole

https://huagongshe.com/reaction/53663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(2R, 3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidino)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol p-toluenesulfonateHCID 88342129—
SolventDiethyl EtherHCID 3283—
ProductEfinaconazoleHCID 48918174.3%

Reaction Steps

To 18.3 g of the p-toluenesulfonate obtained above there were added 40 ml of ethyl ether and 35 ml of 1N aqueous solution of sodium hydroxide. The organic phase was taken out, and dried over 5 g of anhydrous magnesium sulfate and then the solvent was removed. There was added 40 ml of n-hexane to the residual liquid, and the precipitated crystal was separated by filtration, and dried to obtain 9.43 g of the desired (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidine-1-yl)-1-(1H-1,2,4-triazole-1-yl)butane-2-ol. 1H-NMR spectrum of this compound coincided with that of the compound in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620994
Source datasetuspto-grants-1997_04
ORD IDord-95f26bcfff1f42f7ba8d95bf590a9d25
Source noteuspto-grants-1997_04