반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[C:3]=1[CH:4]=O.Cl.[NH2:12][OH:13].[OH-].[Na+].C(=O)C1C=CC=CC=1>O.CO>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[C:3]=1[CH:4]=[N:12][OH:13]참가 물질
7
실험 절차
2,6-Dichloro-benzaldehyde (7.0 g, 40 mmol) and hydroxylamine hydrochloride (2.16 g, 44 mmol) are added to 10 mL of water and 30 mL of methanol. Sodium hydroxide (4.0 g, 100 mmol) is dissolved in 8 mL of water slowly. The sodium hydroxide solution is added to the benzaldehyde solution. The reaction is stirred overnight. The reaction mixture is partitioned between ethyl acetate and water. The organic layer is washed with brine and dried over solid sodium sulfate. The organic layer is filtered and the solvent is removed under reduced pressure to yield the title compound.
후처리
- customThe reaction mixture is partitioned between ethyl acetate and water
- washThe organic layer is washed with brine
- dry with materialdried over solid sodium sulfate
- filtrationThe organic layer is filtered
- customthe solvent is removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-91b4da23681b4de2a3466fc951868c49
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08153624B2
연결된 노트
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