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HRID 257407作成日:2026年10月27日

Triethylamine → 1-(3-n-butoxy-2-hydroxypropyl)-5,5-dipropyl-(1H,3H,5H)pyrimidine-2,4,6-trione

https://huagongshe.com/reaction/257407

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Butyl glycidyl etherHCID 17049—
反応物PropylbarbitalHCID 75192—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(3-n-butoxy-2-hydroxypropyl)-5,5-dipropyl-(1H,3H,5H)pyrimidine-2,4,6-trioneHCID 1978312951.6%

反応条件

温度60 °C

反応手順

A solution of 5,5 dipropyl-(1H,3H,5H)-pyrimidine-2,4,6-trione (30.8 g, 0.15 mole) in dimethylformamide (30 ml) containing triethylamine (2.02 g, 0.2 mole) was mixed with butyl glycidyl ether (13 g, 0.1 mole). The mixture was heated at 60° C. for 6 hours. The solution was then diluted with water (150 ml) and extracted with toluene (2×50 ml). The organic layer was separated, washed with water (2×100 ml) dried and extracted with 5% aqueous sodium carbonate (6×100 ml). The toluene phase was then extracted with 1M aqueous sodium hydroxide (2×100 ml), the aqueous layers separated, washed with toluene (100 ml) and the pH was adjusted to 3 with sulphuric acid. The precipitated oily product was extracted with toluene (100 ml), and the organic layer was separated, washed with water, dried and evaporated to yield the title compound (16.3 g; 51.6%); purity by HPLC 96.5%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262402
出典データセットuspto-grants-1993_11
ORD IDord-1bb05ed9d92a4f0dad6b0a004d77fbae
出典メモuspto-grants-1993_11