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Sodium Hydroxide → 2-(6-Chloro-2-pyridinyl)-1-(3-methyl-2-furyl)ethanone oxime

HRID 1269064
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HRID 1269064 반응식
[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][C:9]([C:11]2[O:12][CH:13]=[CH:14][C:15]=2[CH3:16])=O)[CH:5]=[CH:4][CH:3]=1.Cl.[NH2:18][OH:19].[OH-].[Na+]>CO>[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][C:9]([C:11]2[O:12][CH:13]=[CH:14][C:15]=2[CH3:16])=[N:18][OH:19])[CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 184466082-(6-Chloro-2-pyridinyl)-1-(3-methyl-2-furyl)ethanone

생성물 1

HCID 858395372-(6-Chloro-2-pyridinyl)-1-(3-methyl-2-furyl)ethanone oxime수율 52.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 2-(6-chloro-2-pyridinyl)-1-(3-methyl-2-furyl)ethanone (52.2 g, 221 mmol) in methanol (500 mL) was added hydroxylamine hydrochloride (76.96 g, 1.11 mol) followed by an aqueous solution of sodium hydroxide (44.3 g, 1.11 mol). The resultant suspension was heated at reflux for 2 hours and then cooled to room temperature. The mixture was concentrated and water was added to the residue while stirring. After stirring for 20 minutes, a white solid precipitated. This solid was collected by filtration and washed with water to give 2-(6-chloro-2-pyridinyl)-1-(3-methyl-2-furyl)ethanone oxime (29.0 g, 52%) as a white solid. 1H NMR (CDCl3): δ 7.54 (t, 1H), 7.31 (s, 1H), 7.15 (d, 1H), 7.10 (d, 1H), 6.28 (s, 1H), 4.34 (s, 2H), 2.22 (S 3H). MS m/z 273 (M+1).

후처리

  1. temperatureat reflux for 2 hours
  2. concentrationThe mixture was concentrated
  3. additionwater was added to the residue
  4. stirringAfter stirring for 20 minutes
  5. customa white solid precipitated
  6. filtrationThis solid was collected by filtration
  7. washwashed with water

출처 및 근거

ORD 기록
ord-6906286ae029476d95463ad3998bbc4d
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07199120B2

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