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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333975Generated: October 30, 2026

Hydrochloric Acid → Ethyl 4,4,5,5-tetrafluoro-3-hydroxy-pentanoate

https://huagongshe.com/reaction/333975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4,4,5,5-tetrafluoro-3-oxo-pentanoateHCID 13356428—
SolventTolueneHCID 1140—
ProductEthyl 4,4,5,5-tetrafluoro-3-hydroxy-pentanoateHCID 8669116488,235.297%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 4,4,5,5-tetrafluoro-3-oxo-pentanoate (25.7 g, 0.119 mmol) was dissolved in toluene (260 ml) and cooled to 0° C. Sodium borohydride (5.4 g, 0.143 g) was added portionwise, and the mixture was allowed to reach room temperature overnight with stirring. The mixture was then cooled to 0° C. and acidified with 1 m HCl. The phases were separated, the aqueous phase was extracted two times with ethyl acetate, the combined organic phases were dried over magnesium sulfate and the solvent was removed under reduced pressure. The residue was dissolved in a minimum amount of methanol, the resulting solution was evaporated to dryness under reduced pressure to yield 22.9 g of a residue (0.105 mol, 88%) that were used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-76f5c52579a347a580377e478a065673
Source noteuspto-grants-2014_11