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Hydrochloric Acid → N-(2-chloro-3-methoxyphenyl)-2-hydroxyimino-acetamide

HRID 388684
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HRID 388684 반응식
S([O-])([O-])(=O)=O.[Na+].[Na+].Cl[C:9](Cl)(Cl)[CH:10]([OH:12])O.Cl.[Cl:16][C:17]1[C:23]([O:24][CH3:25])=[CH:22][CH:21]=[CH:20][C:18]=1[NH2:19].Cl.[NH2:27][OH:28]>O>[Cl:16][C:17]1[C:23]([O:24][CH3:25])=[CH:22][CH:21]=[CH:20][C:18]=1[NH:19][C:10](=[O:12])[CH:9]=[N:27][OH:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 787HydroxylamineHCID 2707Chloral HydrateHCID 24436Sodium SulfateHCID 248201302-Chloro-3-methoxyaniline hydrochloride

생성물 1

HCID 86633207N-(2-chloro-3-methoxyphenyl)-2-hydroxyimino-acetamide

시약·촉매·용매 1

HCID 962
Water
용매
2회

실험 절차

To a stirred solution of sodium sulfate (58.5 g, 412 mmol) in water (100 mL) was added a solution of chloralhydrate (9.36 g, 56.6 mmol) in water (120 mL). Chloroanisidine 215d (10 g, 51.5 mmol) was added followed by 37% HCl (20 mL). A solution of hydroxylamine (50% in water, 4.7 mL, 154.5 mmol) in 50 mL was then added and the reaction mixture was refluxed for 90 min. The suspended solid was filtered off, and washed with water and ether. Organics were dried over Na2SO4, filtered, and concentrated under reduced pressure to yield compound 245d as a brown solid. 1H NMR (DMSO-d6, 400 MHz) δ (ppm) 3.86 (s, 3H), 6.98 (d, J=8.07 Hz, 1H), 7.31 (t, J=8.07 Hz, 1H), 7.61 (d, J=8.07 Hz, 1H), 7.66 (s, 1H), 9.43 (s, 1H), 12.43 (s, 1H).

후처리

  1. temperaturethe reaction mixture was refluxed for 90 min
  2. filtrationThe suspended solid was filtered off
  3. washwashed with water and ether
  4. dry with materialOrganics were dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3894ded36a25460f8c01b253f3c5bce7
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377962B2

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