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N,N'-Dimethylethylenediamine → 2-(2-methoxyphenyl)-1,3-dimethylimidazolidine

HRID 2111946
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HRID 2111946 반응식
[CH:1](=O)[C:2]1[C:3]([O:8][CH3:9])=[CH:4][CH:5]=[CH:6][CH:7]=1.[CH3:11][NH:12][CH2:13][CH2:14][NH:15][CH3:16].[O-]S([O-])(=O)=O.[Mg+2]>C(O)C>[CH3:9][O:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[CH:1]1[N:15]([CH3:16])[CH2:14][CH2:13][N:12]1[CH3:11]
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참가 물질

5

반응물 3

HCID 8070N,N'-DimethylethylenediamineHCID 86582-MethoxybenzaldehydeHCID 24083Sulfuric acid magnesium salt (1:1)

생성물 1

HCID 41442452-(2-methoxyphenyl)-1,3-dimethylimidazolidine수율 88%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of o-anisaldehyde (9.0 g, 66 mmol) and N,N′-dimethylethylenediamine (7.9 mL, 73 mmol) in ethanol (180 mL) was stirred at r.t. for overnight. MgSO4 (30 g) was added and the mixture was stirred for 20 min. The reaction mixture was filtered and washed with ether. The solvent was removed in vacuo to afford 2-(2-methoxyphenyl)-1,3-dimethylimidazolidine as a light yellow solid, 12 g, yield 88%. 1H NMR (500 MHz, CHLOROFORM-D) δ ppm 2.21 (s, 6H) 2.57-2.72 (m, 2H) 3.34 (d, J=2.75 Hz, 2H) 3.82 (s, 3H) 4.13 (s, 1H) 6.88 (d, J=8.24 Hz, 1H) 7.00 (t, J=7.48 Hz, 1H) 7.25-7.30 (m, 1H) 7.67 (d, J=7.63 Hz, 1H).

후처리

  1. filtrationThe reaction mixture was filtered
  2. washwashed with ether
  3. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-46efad6ca50340efa39227445f5943a8
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07521441B2

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