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HRID 21751作成日:2026年10月26日

Methanol → Methyl 5-oxo-L-prolinate

https://huagongshe.com/reaction/21751

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sulfuric AcidHCID 1118—
反応物L-Pyroglutamic AcidHCID 7405—
反応物Sodium SulfateHCID 24436—
反応物Sodium BicarbonateHCID 516892—
生成物Methyl 5-oxo-L-prolinateHCID 78646—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424444
出典データセットuspto-grants-1995_06
ORD IDord-bcac725e8d74422aad39a80a0f9d319a
出典メモuspto-grants-1995_06