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HRID 7285作成日:2026年10月23日

Ethyl Acetate → Dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioate

https://huagongshe.com/ja/reaction/7285

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Benzyl chloroformateHCID 10387—
反応物D-Glutamic AcidHCID 23327—
反応物Thionyl ChlorideHCID 24386—
反応物Potassium BicarbonateHCID 516893—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioateHCID 86606597—

反応手順

Thionyl chloride (30 ml) was added to a cooled solution of D-glutamic acid (33.2 g) in methanol (250 ml) and the mixture subsequently heated under reflux for 16 h. On cooling, the mixture was concentrated under reduced pressure and the residue azeotroped with toluene to give a white solid. This was stirred with ethyl acetate, water and potassium hydrogen carbonate at 0° C. while benzyl chloroformate (30 ml) was added. The mixture was warmed to room temperature and stirred for 5 h. The separated organic phase was washed with water, dried (over magnesium sulphate) and concentrated under reduced pressure to provide a yellow oil. This oil was purified using flash column chromatography (silica, eluting with cyclohexane:ethyl acetate 2:1) to give the title compound (22.45 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084139B2
出典データセットuspto-grants-2006_08
ORD IDord-0d66f2913bdf4cf684ad6583f5f27c4b
出典メモuspto-grants-2006_08