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HRID 1644710作成日:2026年10月25日

Citric Acid → 2-Ethoxycarbonyl-3-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-4-methyl-pentanedioic acid 1-tert-butyl ester 5-ethyl ester

https://huagongshe.com/reaction/1644710

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物tert-Butyl ethyl malonateHCID 96345—
反応物HCID 11481404HCID 11481404—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylacetamideHCID 31374—
生成物2-Ethoxycarbonyl-3-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-4-methyl-pentanedioic acid 1-tert-butyl ester 5-ethyl esterHCID 59326554—

反応条件

温度25 °C

反応手順

Malonic acid tert-butyl ester ethyl ester (30.08 g, 151.8 mmol) was added to a solution of potassium tert-butoxide (16.30 g, 138.0 mmol) in 200 mL of N,N-dimethyl acetamide, while the reaction temperature was maintained at ˜25° C. To the resulting mixture was then added the solution of 4-(4-fluoro-phenyl)-2-methyl-buta-2,3-dienoic acid ethyl ester prepared above, at such a rate that the reaction temperature was maintained between 20-28° C. After the addition was complete, the reaction mixture was stirred at room temperature for 20 minutes, when HPLC indicated completed reaction. The mixture was then treated with 100 mL of 1M citric acid and 150 mL of ice-water, and then extracted with 400 mL of methyl tert-butyl ether. The organic extract was separated and washed with 2×200 mL of water, and then concentrated to produce 56.36 g of a yellow oil, which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124629B2
出典データセットuspto-grants-2012_02
ORD IDord-2756807afef94cedbe33fd59b19713b7
出典メモuspto-grants-2012_02