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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257407생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/257407

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Butyl glycidyl etherHCID 17049—
반응물PropylbarbitalHCID 75192—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(3-n-butoxy-2-hydroxypropyl)-5,5-dipropyl-(1H,3H,5H)pyrimidine-2,4,6-trioneHCID 1978312951.6%

반응 조건

온도60 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262402
출처 데이터셋uspto-grants-1993_11
ORD IDord-1bb05ed9d92a4f0dad6b0a004d77fbae
출처 메모uspto-grants-1993_11