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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733384Generated: October 30, 2026

Hydrochloric Acid → ethyl (3R)-3-hydroxybutanoate

https://huagongshe.com/reaction/733384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetoacetateHCID 8868—
ReactantHCID 178418361HCID 178418361—
CatalystRutheniumHCID 23950—
SolventEthanolHCID 702—
Productethyl (3R)-3-hydroxybutanoateHCID 440030—

Reaction Conditions

Temperature80 °C

Reaction Steps

30 g of ethyl acetoacetate, 5 ml of degassed ethanol and 0.9 ml of 1 N HCl are introduced in succession into a Schlenk vessel filled with argon. This solution and the catalyst solution from Example C1 are then transferred in succession by means of a steel capillary into a 50 ml steel autoclave filled with argon. The s/c (substrate/catalyst) ratio is 75 000. The autoclave is closed and a pressure of 50 bar is set using 4 flushing cycles (pressurization with 20 bar of hydrogen). The autoclave is then heated to 80° C., and after 30 minutes the reaction pressure is set to 80 bar. The autoclave is stirred for 19 hours. The heating is subsequently switched off and the autoclave is cooled to room temperature. After depressurization, a reddish reaction solution is isolated. The conversion is >98% (determined by means of GC and 1H-NMR). Removal of the solvent on a rotary evaporator gives a quantitative yield of ethyl (R)-3-hydroxybutyrate having an enantiomeric purity of 97.1% ee. (determined by means of GC after reaction with trifluoroacetic anhydride; column: Lipodex E, 50 m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589196B2
Source datasetuspto-grants-2009_09
ORD IDord-9fdef5d4717d453b964952959d1c2e11
Source noteuspto-grants-2009_09