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

HRID 730031
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인쇄 미리보기

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HRID 730031 반응식
C([O-])(=O)C.[Na+].Cl.[NH2:7][OH:8].[F:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][C:17]([C:19]2[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=2)=O)=[CH:12][CH:11]=1>CO>[F:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][C:17]([C:19]2[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=2)=[N:7][OH:8])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 110421332-(4-Fluorophenyl)-1-(pyridin-4-yl)ethanone

생성물 1

HCID 1362276032-(4-Fluorophenyl)-1-pyridin-4-ylethanone oxime

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Sodium acetate (36.1 g; 0.44 mol) and hydroxylamine hydrochloride (22.0 g; 0.32 mol) were introduced into a suspension of a2 (21.5 g; 0.1 mol) in 50% strength methanol (350 ml). The reaction mixture was stirred under reflux for 1 h. When the clear solution was cooled in an ice bath, a3 was obtained as a beige precipitate which was filtered off, washed with H2O and dried under reduced pressure over P2O5.

후처리

  1. temperatureunder reflux for 1 h
  2. temperatureWhen the clear solution was cooled in an ice bath

출처 및 근거

ORD 기록
ord-f4fed1cec8154e5c9649459db57a5819
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582660B2

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