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HRID 532105作成日:2026年10月25日

Iodoethane → N-(3-(3-(Dimethylamino)-1-oxo-2-propenyl)phenyl)-N-ethylacetamide

https://huagongshe.com/reaction/532105

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Sodium hydrideHCID 24758—
反応物N-[3-(3-Dimethylaminoacryloyl)phenyl]acetamideHCID 53412415—
溶媒DimethylformamideHCID 6228—
生成物N-(3-(3-(Dimethylamino)-1-oxo-2-propenyl)phenyl)-N-ethylacetamideHCID 53395302—

反応手順

A mixture of N-{3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl}acetamide 2 (12.7 g, 0.055 mol) and sodium hydride (60% in oil) (2.5 g) in DMF (150 ml) under nitrogen was stirred at room temperature for 30 minutes. The solution was then cooled to 0° C., and a solution of ethyl iodide (9.38 g, 0.063 mol) in DMF (50 ml) was added slowly dropwise. The mixture was then stirred at room temperature for one hour. The DMF was removed under high vacuum, water (200 ml) was added to the residue and the mixture was extracted with ethyl acetate (2×200 ml). The combined ethyl acetate extracts were washed with water (150 ml) and brine (100 ml), dried over sodium sulfate, filtered and concentrated to dryness to give the crude product. Compound 5 was obtained after recrystallization from hexane (7.9 g). M. P. (Hexane): 109-112° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08852953B2
出典データセットuspto-grants-2014_10
ORD IDord-29d93695660641eab5109be1e1ecc033
出典メモuspto-grants-2014_10