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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257406생성일: 2026년 10월 26일

Sulfuric Acid → 1-(3-n-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trione

https://huagongshe.com/reaction/257406

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물PhenobarbitalHCID 4763—
반응물TriethylamineHCID 8471—
반응물2-Propanol, 1-butoxy-3-chloro-HCID 27759—
용매DimethylformamideHCID 6228—
생성물1-(3-n-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trioneHCID 1978312453.1%

반응 단계

A solution of phenobarbital (69.6 g, 0.3 mole) in dimethylformamide (60 ml) containing triethylamine (20.2 g, 0.2 mole) was stirred with 1-chloro-3-n-butoxy-2-propanol (33.2 g, 0.2 mole) for 6 hours at 70° C. The reaction mixture was then poured into 3% sulphuric acid (500 ml) and the precipitated product was extracted with toluene (200 ml) at 70° C. The toluene layer was separated, washed with 3% aqueous sulphuric acid (200 ml) and left overnight at 4° C. The precipitated phenobarbital was filtered off and filtrate extracted with 5% aqueous sodium carbonate (5×100 ml). The organic layer was then extracted with 1M aqueous sodium hydroxide (2×200 ml), the aqueous layers collected, washed with toluene (100 ml) and the pH was adjusted to 3 with sulphuric acid. The precipitated product was extracted with toluene (150 ml), the organic layer was separated, dried and evaporated under reduced pressure to give the title compound (38.5 g, 53%); purity by HPLC 96.5% .

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262402
출처 데이터셋uspto-grants-1993_11
ORD IDord-e726e6ac9f05453f95faec9db4973de4
출처 메모uspto-grants-1993_11