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Hydroxyamine hydrochloride → 1-(4-Fluorophenyl)-2-pyridin-2-ylethanone Oxime

HRID 2300190
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HRID 2300190 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1.Cl.[NH2:18][OH:19].C([O-])(=O)C.[Na+]>CO.O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[N:18][OH:19])[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 36168691-(4-Fluorophenyl)-2-pyridin-2-ylethanone

생성물 1

HCID 880148471-(4-Fluorophenyl)-2-pyridin-2-ylethanone Oxime수율 87.3%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water
용매

실험 절차

To a solution of 1-(4-fluorophenyl)-2-pyridin-2-ylethanone (6.27 g 29 mmol) in methanol (100 ml) was added a solution of hydroxylamine hydrochloride (9.6 g 130 mmol) and sodium acetate (15.6 g) in water (80 ml) and the reaction was stirred at room temperature for 24 hours. The resulting precipitate was filtered off and dried to give the title compound as a white solid (5.83 g 87%). (M-H2O)H+: 213; NMR: (CDCl3): δ 4.42 (2H, s) 7.00 (2H, t) 7.14 (1H, m) 7.28 (1H, d) 7.59 (1H, dt) 7.72 (2H, m) 8.55 (1H, m) 8.96 (1H, br).

후처리

  1. filtrationThe resulting precipitate was filtered off
  2. customdried

출처 및 근거

ORD 기록
ord-3eb63e4daa7647e39e34d9153ae39000
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06498166B1

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