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HRID 22971作成日:2026年10月25日

Sodium hydride → HCID 12132856、化合物

https://huagongshe.com/reaction/22971

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Dimethyl (2-oxoheptyl)phosphonateHCID 580181—
反応物[(Z)-4-((R)-2-formyl-5-oxo-pyrrolidin-1-yl)-but-2-enyloxy]-acetic acid ethyl esterHCID 12132855—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物HCID 12132856HCID 12132856—

反応手順

To a solution of sodium hydride (95%, 0.02 g, 0.78 mmol) in 10 mL of anhydrous 1,2-dimethoxyethane at 0° C. under a nitrogen atmosphere was added dimethyl 2-oxoheptylphosphonate (0.17 mL, 0.78 mmol), and the reaction was stirred for 1 hour. A solution of [(Z)-4-((R)-2-formyl-5-oxo-pyrrolidin-1-yl)-but-2-enyloxy]-acetic acid ethyl ester (0.21 g, 0.78 mmol) in 2 mL anhydrous 1,2-dimethoxyethane was added. The reaction was allowed to come to room temperature, stirred for 3 hours and then quenched with an aqueous solution of saturated ammonium chloride. After extraction with ethyl acetate, the organic solution was dried (brine, Na2SO4), evaporated and purified by chromatography to yield {(Z)-4-[(R)-2-oxo-5-((E)-3-oxo-oct-1-enyl)-pyrrolidin-1-yl]-but-2-enyloxy}-acetic acid ethyl ester as an oil. This material was taken directly on to the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849657B2
出典データセットuspto-grants-2005_02
ORD IDord-d46a0295b2bc4e8c8922c2c4c63235b6
出典メモuspto-grants-2005_02