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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21751Generated: October 26, 2026

Methanol → Methyl 5-oxo-L-prolinate

https://huagongshe.com/reaction/21751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantL-Pyroglutamic AcidHCID 7405—
ReactantSodium SulfateHCID 24436—
ReactantSodium BicarbonateHCID 516892—
ProductMethyl 5-oxo-L-prolinateHCID 78646—

Reaction Conditions

Temperature60 °C

Reaction Steps

Methanol (62 L, 1.155 mol), L-pyroglutamic acid (20 kg, 154.9 mol) and H2SO4 (97%, 0.87 L, 15.5 mol) were introduced into a reactor. The suspension was warmed to 60° C. and stirred until the pyroglutamic acid concentration dropped below 10%. The temperature of the reactor jacket was lowered to 0° C., and when the internal temperature reached 30° C., 9.7 kg (68.1 mol) of Na2SO4 was added and stirred for 15 min, then 8.1 kg (96.4 mol) of NaHCO3 was added. When pH 7 was reached (about 10 min), the suspension was filtered over a pad of celite. The filtrate was reintroduced into the reactor, and the methanol was distilled off at a pressure of 90-160 mbar and a jacket temperature of 50° C. Ethyl acetate (53 L) was then added with stirring, the mixture cooled to 0° C., and the mixture stirred for 16 hr. Unreacted pyroglutamic acid crystallized out and was removed by filtration. Removal of the ethyl acetate by evaporation under reduced pressure provided the title product as a viscous yellow oil, which was taken to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424444
Source datasetuspto-grants-1995_06
ORD IDord-bcac725e8d74422aad39a80a0f9d319a
Source noteuspto-grants-1995_06