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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | Methyl 3-hydroxybutyrate, (R)- | HCID 2724279 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olide | HCID 54688321 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05625059 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-ecd6a5b30a544048af33089764496ebf |
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| Source note | uspto-grants-1997_04 |
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