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Methylamine → (1-Methyl-4-phenyl-1H-imidazol-5-YL)methanol

HRID 32507
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HRID 32507 반응식
[CH3:1][NH2:2].C1O[CH:7]([OH:9])[CH2:6]OC1O.[N+:11]([CH:13]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)S(C1C=CC(C)=CC=1)(=O)=O)#[C-:12]>C1COCC1>[CH3:1][N:2]1[C:6]([CH2:7][OH:9])=[C:13]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[N:11]=[CH:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6329MethylamineHCID 186078Glycolaldehyde dimerHCID 10967613a-Tosylbenzyl isocyanide

생성물 1

HCID 17965886(1-Methyl-4-phenyl-1H-imidazol-5-YL)methanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Methylamine (33% in industrial methylated spirits, 60.3 mL) was added to a solution of glycolaldehyde dimer (2.7 g) in THF (320 mL). After 75 minutes 1-{[isocyano(phenyl)methyl]sulfonyl}-4-methylbenzene (PhTosMIC) (Org. Syn., 77, 198-205) (10.8 g) was added, cooling to keep the reaction temperature below 30° C. The reaction was stirred for 90 minutes and the solvent evaporated to a volume of 100 mL. Water (500 mL) was added, and the title compound (4.94 g, 66%) collected by filtration as a white solid. The filtrate was extracted into EtOAc, dried, and the solvent removed in vacuo. The residue was triturated with EtOAc to give a further 1.06 g (14%) as a white solid.

후처리

  1. temperaturecooling
  2. customthe reaction temperature below 30° C
  3. customthe solvent evaporated to a volume of 100 mL
  4. additionWater (500 mL) was added
  5. filtrationthe title compound (4.94 g, 66%) collected by filtration as a white solid
  6. extractionThe filtrate was extracted into EtOAc
  7. customdried
  8. customthe solvent removed in vacuo
  9. customThe residue was triturated with EtOAc
  10. customto give a further 1.06 g (14%) as a white solid

출처 및 근거

ORD 기록
ord-8a42de69d6014efaa40cce829552abd2
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07427616B2

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