반응식
[OH:1][NH:2][C:3]([NH2:5])=[O:4].[C:6]([CH2:9][C:10](=O)[CH3:11])(=O)[CH3:7].[ClH:13]>>[ClH:13].[CH3:7][C:6]1[N:5]=[C:3]([OH:4])[N+:2]([O-:1])=[C:10]([CH3:11])[CH:9]=1참가 물질
반응 조건
- 온도
- 2 °C
실험 절차
0.40 mol (30.6 g) hydroxy urea was dissolved in 600 ml of 1 M HCl and 0.50 mol (50.06 g) acetyl acetone were added dropwise under ice cooling, maintaining the internal temperature at 1-3° C. The solution was thawed to room temperature in an ice bath and stirred over night, then filtered off and evaporated to dryness. The residue was suspended with 400 ml of acetone, the mixture was cooled to −18° C., the solid filtered off and washed with a little ice-cold acetone. After drying, 45.5 g of crude product were obtained. The crude product was recrystallized with 4.0 l ethanol from the boiling heat, cooled to −18° C., filtered off and washed with little ethanol and dried (fraction 1). The mother liquor was concentrated on a rotary evaporator until product started to precipitate again, cool stored and a second fraction isolated. After drying 26.0 g (1. fraction, purity>98%) and 11.0 g (2. fraction, contained 32% NH4Cl as by-product) of the title compound was obtained.
후처리
- customThe solution was thawed to room temperature in an ice bath
- filtrationfiltered off
- customevaporated to dryness
- temperaturethe mixture was cooled to −18° C.
- filtrationthe solid filtered off
- washwashed with a little ice-cold acetone
- customAfter drying
출처 및 근거
- ORD 기록
- ord-7deaf9cff9b84ea8bf6f17838ae18696
- 출처 데이터셋
- uspto-grants-2016_08
- 특허 번호
- US09422247B2
연결된 노트
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