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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Phenobarbital | HCID 4763 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Propanol, 1-butoxy-3-chloro- | HCID 27759 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(3-n-Butoxy-2-hydroxypropyl)-5-ethyl-5-phenyl-(1H,3H,5H)-pyrimidine-2,4,6-trione | HCID 19783124 | 53.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05262402 |
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| 출처 데이터셋 | uspto-grants-1993_11 |
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| ORD ID | ord-e726e6ac9f05453f95faec9db4973de4 |
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| 출처 메모 | uspto-grants-1993_11 |
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