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HRID 230384作成日:2026年10月26日

Dimethylformamide → HCID 178444001、化合物

https://huagongshe.com/reaction/230384

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Cesium carbonateHCID 10796—
反応物Ammonium AcetateHCID 517165—
反応物2-Bromo-1-(3-bromophenyl)ethan-1-oneHCID 519585—
反応物2-(((Tert-butoxy)carbonyl)amino)-6-methylheptanoic acidHCID 53650046—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒O-XyleneHCID 7237—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178444001HCID 17844400163%

反応条件

温度23 °C

反応手順

A mixture of 2-((tert-butoxycarbonyl)amino)-6-methylheptanoic acid (3.5 g; 0.0135 mol) and cesium carbonate (4.89 g; 0.015 mol) in 100 ml ethanol was agitated at about 23° C. for about 1 hour. The ethanol was eliminated by evaporation under reduced pressure in a rotative evaporator. The mixture obtained was dissolved in 100 ml of dimethylformamide and 3-bromophenacyl bromide (3.75 g; 0.0135 mol) was then added. After about 16 hours agitation, the solvent was evaporated under reduced pressure. The mixture obtained was taken up in ethyl acetate and the cesium bromide was then filtered. The ethyl acetate of the filtrate was evaporated and the reaction oil was taken up in a mixture of xylene (100 ml) and ammonium acetate (46.2 g; 0.6 mol). The mixture was then heated to reflux for about one hour and a half and, after cooling, a mixture of icy water and ethyl acetate was poured in the reaction medium. After phase separation, the organic phase was washed with a sodium saturated bicarbonate solution, dried over magnesium sulfate and then evaporated under vacuum. The solid obtained was filtered and then washed with ether to produce a white powder (yield of 63%). Melting point: 134-136° C. MH+=436.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566734B2
出典データセットuspto-grants-2009_07
ORD IDord-bed07fd92cf8416a90801ca326e0ddad
出典メモuspto-grants-2009_07