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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333073Generated: October 29, 2026

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

https://huagongshe.com/reaction/333073

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 86691164—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 4,4,5,5-tetrafluoro-3-oxo-pentanoate (25.7 g, 0.119 mol) was dissolved in toluene (260 ml) and cooled to 0° C. Sodium borohydride (5.4 g, 0.143 mol) 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 1M 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 reduced under reduced pressure. The residue was dissolved in a minimum amount of methanol and evaporated to dryness under reduced pressure to yield 22.9 g (0.105 mol, 88%) that were used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877934B2
Source datasetuspto-grants-2014_11
ORD IDord-6c11e16691494cbc8fd8f84292e0e77b
Source noteuspto-grants-2014_11