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N-2-Naphthalenylacetamide → HCID 13663774, 화합물

HRID 1270748
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HRID 1270748 반응식
[C:1]([NH:4][C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=1)(=[O:3])[CH3:2].[F:15][B-](F)(F)F.F[B-](F)(F)F.ClC[N+]12CC[N+](F)(CC1)CC2>CCOC(C)=O>[F:15][C:6]1[C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH:13]=[CH:14][C:5]=1[NH:4][C:1](=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11394N-2-NaphthalenylacetamideHCID 2724933Selectfluor

생성물 1

HCID 13663774HCID 13663774, 화합물

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 1.95 g (10 mmol) of 2-acetylaminonaphthalene, and 7.1 g (20 mmol) of 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor®) in 30 mL of CH2CN is heated to reflux under an atmosphere of nitrogen for 24 hours. After cooling to room temperature, 50 mL of EtOAc is added and the mixture is washed with H2O and dried over MgSO4. Evaporation of the solvents gives a syrup that is purified by flash chromatography on silica gel (25% EtOAc/hexane) to give 1-fluoro-2-acetylaminonaphthalene.

후처리

  1. temperatureis heated
  2. temperatureto reflux under an atmosphere of nitrogen for 24 hours
  3. washthe mixture is washed with H2O
  4. dry with materialdried over MgSO4
  5. customEvaporation of the solvents
  6. customgives a syrup that
  7. customis purified by flash chromatography on silica gel (25% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-419799cfae6d4c5691385fcab24fa48d
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07202364B2

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