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2-Chloropropane → HCID 15067843、化合物

HRID 1085462
ノート
印刷プレビュー

反応式

HRID 1085462 の反応式
Cl[CH:2]([CH3:4])[CH3:3].[Mg].[C:6]1([C:12]2[NH:13][C:14]([CH3:19])=[C:15]([CH:17]=[O:18])[N:16]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>C1COCC1>[C:6]1([C:12]2[NH:13][C:14]([CH3:19])=[C:15]([CH:17]([OH:18])[CH:2]([CH3:4])[CH3:3])[N:16]=2)[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 63612-ChloropropaneHCID 5462224MagnesiumHCID 135486495-Methyl-2-phenyl-1h-imidazole-4-carbaldehyde

生成物 1

HCID 15067843HCID 15067843、化合物収率 57.9%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

35 Grams (0.45 mol) of 2-chloropropane was added to 10.8 g (0.45 mol) of magnesium in 100 ml of diethyloxyde. Then 55.8 g (0.3 mol) of 2-phenyl-4-formyl-5-methyl-1H-imidazole in 100 ml of THF were added. At the end of the addition, the mixture was refluxed for 30 minutes and then cooled and poured on ice water. The aqueous layer was extracted twice with 100 ml of diethyl ether. Evaporation of the solvent gave a residue which was recrystallized in ethanol to yield 40 grams of 2-phenyl-4-(1-hydroxy-2-methylpropyl)-5-methyl-1H-imidazole, which melted at 214° C.

後処理

  1. additionAt the end of the addition
  2. temperaturethe mixture was refluxed for 30 minutes
  3. temperaturecooled
  4. additionpoured on ice water
  5. extractionThe aqueous layer was extracted twice with 100 ml of diethyl ether
  6. customEvaporation of the solvent
  7. customgave a residue which
  8. customwas recrystallized in ethanol

出典と根拠

ORDレコード
ord-2a48a59f0e6543e5bec3964dd0d6da25
出典データセット
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05010075

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート