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Hydroxyamine hydrochloride → 2-Chloro-6-(4-pyridyl)benzaldoxime

HRID 1241920
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인쇄 미리보기

반응식

HRID 1241920 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[C:3]=1[CH:4]=O.Cl.[NH2:17][OH:18]>N1C=CC=CC=1>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[C:3]=1[CH:4]=[N:17][OH:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 219376462-Chloro-6-(4-pyridyl)benzaldehyde

생성물 1

HCID 1363341222-Chloro-6-(4-pyridyl)benzaldoxime수율 99%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2-Chloro-6-(4-pyridyl)benzaldehyde (80 mg, 0.37 mmol) was dissolved in pyridine (2 mL) at room temperature. Hydroxylamine hydrochloride (26 mg, 0.38 mmol) was added and the mixture was allowed to stir overnight. The mixture was then concentrated under reduced pressure to obtain 2-chloro-6-(4-pyridyl)benzaldoxime (85 mg, 99% yield). MW=233 confirmed by LC-MS, tr=8.36 min (Method Y) MH+=231–235

후처리

  1. concentrationThe mixture was then concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-6826822b0fac4c448f64999aae1ecf01
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07115642B2

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