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Nitrosobenzene → (E)-N-hydroxy-2-methyl-N,3-diphenylacrylamide

HRID 1099338
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인쇄 미리보기

반응식

HRID 1099338 반응식
C1CCN2C(=NCCC2)CC1.[CH3:12]/[C:13](=[CH:16]\[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)/[CH:14]=[O:15].[N:23]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:24]>ClCCl>[OH:24][N:23]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:14](=[O:15])/[C:13](/[CH3:12])=[CH:16]/[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11473NitrosobenzeneHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 5372813alpha-METHYLCINNAMALDEHYDE

생성물 1

HCID 25115717(E)-N-hydroxy-2-methyl-N,3-diphenylacrylamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

DBU (15 mg, 0.1 mmol) was added under argon to a solution of (E)-2-methyl-3-phenylacrylaldehyde (146 mg, 1 mmol), nitrosobenzene (107 mg, 1 mmol) and catalyst (36.4 mg, 0.1 mmol) in dichloromethane (5 mL). The reaction mixture was stirred at room temperature for 10 min. The solvent was removed under vacuum, and the residue was purified by flash silica gel column chromatography using hexane and ethyl acetate as the eluents.

후처리

  1. customThe solvent was removed under vacuum
  2. customthe residue was purified by flash silica gel column chromatography

출처 및 근거

ORD 기록
ord-3c3bd15da93b4e7485fed6a1e075a7de
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08143423B2

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