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Benzaldehyde → HCID 25115948, 화합물

HRID 1099345
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반응식

HRID 1099345 반응식
C1CCN2C(=NCCC2)CC1.[CH:12](=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[F:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:22]=1[N:28]=[O:29]>ClCCl>[F:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:22]=1[N:28]([OH:29])[C:12](=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 240BenzaldehydeHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 370833629270-54-0

생성물 1

HCID 25115948HCID 25115948, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

DBU (15 mg, 0.1 mmol) was added under argon to a solution of benzaldehyde (106 mg, 1 mmol), 1,3-difluoro-2-nitrosobenzene (143 mg, 1 mmol) and catalyst (36.4 mg, 0.1 mmol) in dichloromethane (5 mL). The reaction mixture was stirred at room temperature for 60 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-9845a078227d46a48a2bbb2a0a23edc9
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08143423B2

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