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

HRID 1418451
ノート
印刷プレビュー

反応式

HRID 1418451 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

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, 0.93M 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.

後処理

  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)

出典と根拠

ORDレコード
ord-bb87282e00ff4ec5a397da25cf51377b
出典データセット
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05883106

反応ノート

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