Hydroxyamine hydrochloride → HCID 86744460, 화합물
반응식
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=1[CH:12]=O.Cl.[NH2:19][OH:20]>N1C=CC=CC=1>[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=1[CH:12]=[N:19][OH:20]참가 물질
4
실험 절차
A solution of 2-[(2,3-dimethylphenyl)amino]benzaldehyde (11 g, 0.049 mol) and hydroxylamine hydrochloride (17 g, 0.25 mol) in pyridine (250 ml) is stirred at room temperature overnight. The solvent is evaporated and the residue is partitioned between ethyl acetate (200 ml) and 10% aqueous HCl (200 ml). The organic layer is washed with 10% aqueous HCl (200 ml) and water (2×100 ml). The organic layer is dried (MgSO4) and the solvent is evaporated to give 2-[(2,3-dimethylphenyl) amino]benzaldehyde oxime which is recrystallized from hexane. Yield 7.3 g (62%); mp 107°-108° C.
후처리
- customThe solvent is evaporated
- customthe residue is partitioned between ethyl acetate (200 ml) and 10% aqueous HCl (200 ml)
- washThe organic layer is washed with 10% aqueous HCl (200 ml) and water (2×100 ml)
- dry with materialThe organic layer is dried (MgSO4)
- customthe solvent is evaporated
출처 및 근거
- ORD 기록
- ord-a268f8f519ef464db6e6acca06f0bf16
- 출처 데이터셋
- uspto-grants-1991_12
- 특허 번호
- US05075330
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