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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419552Generated: October 26, 2026

Quinine → (S)-2-(4-difluoromethoxyphenyl)-3-methylbutyric acid

https://huagongshe.com/reaction/1419552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinineHCID 3034034—
Reactant1-(4-Nitrophenyl)-2-dimethylamino-1,3-propanediolHCID 4430907—
Reactant4-(Difluoromethoxy)-alpha-(1-methylethyl)benzeneacetic acidHCID 13118565—
SolventDiethyl EtherHCID 3283—
Product(S)-2-(4-difluoromethoxyphenyl)-3-methylbutyric acidHCID 13118566—

Reaction Conditions

Temperature0 °C

Reaction Steps

1 part of 2-(4-difluoromethoxyphenyl)-3-methylbutyric acid is dissolved in 1-5 parts (by weight) of solvent comprising an organic solvent such as an aliphatic alcohol, an aromatic hydrocarbon, a keton, a halogenated hydrocarbon, an ether, an ester, or an aliphatic hydrocarbon, etc. After the dissolution is completed, 1-3 moles of resolving agent, an optically active organic base such as 1-(4-nitrophenyl)-2-dimethylamino-1,3-propanediol, quinine, substituted α-aminoethylbenzene and the like, is added. The mixture thus obtained is stirred at -50° C. to 200° C., preferably at 0° C. to reflux temperature of the solvent, for 0.1-100 hours, preferably for 1-10 hours. After the reaction is completed, the reaction mixture is allowed to cool, the solids are then collected by filtration and the filtrate discarded. The solids were added to an aqueous solution of 0.1%-36%, preferably 5%-20%, hydrochloric acid, and heated with stirring at 0° C.-100° C., preferably at 20° C.-50° C., for 0.2-1 hour. Thereafter, the reaction mixture was allowed to cool to room temperature, extracted with organic solvents such as aromatic hydrocarbons, halogenated hydrocarbons, aliphatic hydrocarbons, ethers, ketones, esters and the like, and then remove the solvent in the extract by distillation to give (S)-2-(4-difluoromethoxyphenyl)-3-methylbutyric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886207
Source datasetuspto-grants-1999_03
ORD IDord-be24fcada0634676a2e4d6eac98f92ee
Source noteuspto-grants-1999_03