Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55453Generated: October 26, 2026

Hydrochloric Acid → (R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olide

https://huagongshe.com/reaction/55453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
ReactantDimethyl oxalateHCID 11120—
ReactantMethyl 3-hydroxybutyrate, (R)-HCID 2724279—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product(R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olideHCID 54688321—

Reaction Conditions

Temperature0 °C

Reaction Steps

775 ml of 1.6M n-butyllithium solution in n-hexane are added dropwise within a period of 20 minutes at -25° C. to a solution of 1.27 mol of diisopropylamine in 600 ml of tetrahydrofuran. At -70° C., 70.9 g of (R)-3-hydroxybutyric acid methyl ester are then added dropwise within a period of 30 minutes and, after 1 hour, 70.9 g of oxalic acid dimethyl ester are added dropwise within a period of 40 minutes. After a reaction time of two hours at -60° C., the whole is warmed to 0° C. and acidified to pH 2 with 430 ml of 6N hydrochloric acid. The product is isolated by repeated extraction with ethyl acetate and pre-purified by extraction into aqueous bicarbonate solution, acidification with 6N hydrochloric acid to pH 2.5 and extraction once more with ethyl acetate. The solvent is distilled off and the residue is recrystallised from ether/petroleum ether. [α]D20 =+30.0° (3% in CHCl3), m.p. 94°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05625059
Source datasetuspto-grants-1997_04
ORD IDord-ecd6a5b30a544048af33089764496ebf
Source noteuspto-grants-1997_04