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Methanol → [4-(2-Methylimidazol-1-yl)phenyl]methanol

HRID 1108063
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HRID 1108063 반응식
[CH3:1][C:2]1[N:3]([C:7]2[CH:17]=[CH:16][C:10]([C:11](OCC)=[O:12])=[CH:9][CH:8]=2)[CH:4]=[CH:5][N:6]=1.[H-].C([Al+]CC(C)C)C(C)C.CO.[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+]>C(Cl)Cl>[CH3:1][C:2]1[N:3]([C:7]2[CH:17]=[CH:16][C:10]([CH2:11][OH:12])=[CH:9][CH:8]=2)[CH:4]=[CH:5][N:6]=1
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참가 물질

6

반응물 4

HCID 887MethanolHCID 9357Potassium Sodium TartrateHCID 14664350Ethyl 4-(2-methyl-1H-imidazol-1-yl)benzoateHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 11735617[4-(2-Methylimidazol-1-yl)phenyl]methanol수율 95%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of ethyl 4-(2-methylimidazol-1-yl)benzoate (46 g, 0.2 mol) in dry CH2Cl2 (1 l) cooled to -75° C. under a nitrogen atmosphere was added diisobutyl-aluminum hydride (540 ml, 0.93 M in hexane) carefully over 30 minutes and then the mixture was allowed to warm slowly to ambient temperature. After stirring for 5 hours the reaction mixture was cooled in an ice-bath and methanol (30 ml) carefully added. A 30% aqueous solution of Rochelle's salt (500 ml) was then added and the mixture stirred at ambient temperature for 16 hours. Insolubles (essentially product) were removed by filtration and the organic phase separated and washed with water (500 ml), dried (MgSO4) and evaporated. The combined resultant solids were recrystallized from ethanol (ca 300 ml) to afford the titled compound (35.6 g, 95%) as white needles.

후처리

  1. temperaturewas cooled in an ice-bath
  2. stirringthe mixture stirred at ambient temperature for 16 hours
  3. customInsolubles (essentially product) were removed by filtration
  4. customthe organic phase separated
  5. washwashed with water (500 ml)
  6. dry with materialdried (MgSO4)
  7. customevaporated
  8. customwere recrystallized from ethanol (ca 300 ml)

출처 및 근거

ORD 기록
ord-023c92e845624906a88a32ef8ca33974
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06063928

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