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N-Methoxy-N-methylacetamide → HCID 59208500, 화합물

HRID 2243071
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HRID 2243071 반응식
C([Li])CCC.[CH3:6][O:7][CH2:8][CH2:9][N:10]1[CH:14]=[CH:13][N:12]=[CH:11]1.CON(C)[C:18](=[O:20])[CH3:19]>C1COCC1>[CH3:6][O:7][CH2:8][CH2:9][N:10]1[CH:14]=[CH:13][N:12]=[C:11]1[C:18](=[O:20])[CH3:19]
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참가 물질

5

반응물 3

HCID 537505N-Methoxy-N-methylacetamideHCID 143668401-(2-methoxyethyl)-1H-imidazoleHCID 178418339Butyllithium

생성물 1

HCID 59208500HCID 59208500, 화합물수율 82.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 30 ml (75 mmol) of 2.5 M n-butyllithium in hexanes was added slowly to a solution of 8.48 g (61.3 mmol) 1-(2-methoxyethyl)-1H-imidazole (WO 2003055876 A1) in 200 ml THF cooled in a dry ice-acetone bath. After stirring 1 h, 8 ml (75 mmol) of N-methoxy-N-methylacetamide was added quickly, and the solution was allowed to warm to room temperature over 30 min. After quenching with aqueous NH4Cl, the mixture was diluted with water and extracted twice with EtOAc. The combined EtOAc layers were which washed with brine, dried over anhydrous MgSO4, and concentrated to give an oil that was chromatographed on silica gel (100% DCM followed by gradient elution to 50% EtOAc in DCM). The title compound (8.5 g) was obtained as a mobile oil. MS (ES) (M+H)+: 169 for C8H12CN2O2; NMR: 2.69 (s, 3H), 3.34 (s, 3H), 3.71 (m, 2H), 4.61 (m, 2H), 7.12 (s, 1H), 7.26 (s, 1H).

후처리

  1. temperaturecooled in a dry ice-acetone bath
  2. customAfter quenching with aqueous NH4Cl
  3. additionthe mixture was diluted with water
  4. extractionextracted twice with EtOAc
  5. washwashed with brine
  6. dry with materialdried over anhydrous MgSO4
  7. concentrationconcentrated
  8. customto give an oil that
  9. customwas chromatographed on silica gel (100% DCM followed by gradient elution to 50% EtOAc in DCM)

출처 및 근거

ORD 기록
ord-4ecdeebc4a054d5c81976a3e356c1542
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07674801B2

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