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HRID 257406作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物PhenobarbitalHCID 4763—
反応物TriethylamineHCID 8471—
反応物2-Propanol, 1-butoxy-3-chloro-HCID 27759—
溶媒DimethylformamideHCID 6228—
生成物1-(3-n-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trioneHCID 1978312453.1%

反応手順

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% .

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-e726e6ac9f05453f95faec9db4973de4
出典メモuspto-grants-1993_11