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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086454Generated: November 2, 2026

Acetonitrile → Ethyl 4,4,4-trifluoro-3-hydroxybutanoate

https://huagongshe.com/reaction/2086454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantP-CymeneHCID 7463—
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
SolventTriethylammonium formateHCID 11084032—
ProductEthyl 4,4,4-trifluoro-3-hydroxybutanoateHCID 136210—

Reaction Conditions

Temperature35 °C

Reaction Steps

To 10 mL of acetonitrile were added 5 mL of a mixture of formic acid-triethylamine (5:2 in molar ratio), 7 mg of RuCl[(1R,2R)-p-TsNHCH(C6H5)CH(C6H5)NH2] (p-cymene), and 1.0 g of ethyl 4,4,4-trifluoro-3-oxobutanoate, and the whole was stirred at 35° C. for 15 hours, followed by concentration under reduced pressure using an evaporator. To the resulting concentrate were added 10 mL of water and 10 mL of ethyl acetate, and then a saturated sodium carbonate aqueous solution was added thereto under stirring until the pH became 7 or higher. The ethyl acetate layer separated from the aqueous layer was concentrated to obtain optically active ethyl 4,4,4-trifluoro-3-hydroxybutanoate. Upon the measurement under the above conditions, the optical purity and conversion were found to be 95.0% e.e. and 99.9%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723871B2
Source datasetuspto-grants-2004_04
ORD IDord-7f40b0feb4fe4523a5609b0fb6dfb186
Source noteuspto-grants-2004_04