반응식
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:10][OH:11].[OH-].[Na+]>C(O)C.O>[CH:1](=[N:10]/[OH:11])/[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
6
실험 절차
To a suspension of benzaldehyde (5.30 g, 55 mmol) and hydroxylamine hydrochloride (3.82 g, 55 mmol) in ethanol (4 mL) and water (12 mL) was added ice (23 g). Then a solution of sodium hydroxide (5.0 g, 125 mmol) in water (6 mL) was added dropwise within a 10 min period (temperature rises from −8° C. to +7° C.) whereupon most of the solid dissolves. After 30 min stirring at room temperature a white solid precipitated and the resulting mixture was then diluted with water and acidified with HCl (4 N). The white precipitate was then filtered off, washed with water and dried under high vacuum to afford the title compound (5.31 g, 88%) which was obtained as a colourless liquid. MS m/e (EI): 121.0 [M].
후처리
- dissolutiondissolves
- customprecipitated
- additionthe resulting mixture was then diluted with water
- filtrationThe white precipitate was then filtered off
- washwashed with water
- customdried under high vacuum
출처 및 근거
- ORD 기록
- ord-a5db38ea6cfc499dbab2349b11f21d04
- 출처 데이터셋
- uspto-grants-2008_08
- 특허 번호
- US07414061B2
연결된 노트
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