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Ethylene Glycol → HCID 10517034、化合物

HRID 566549
ノート
印刷プレビュー

反応式

HRID 566549 の反応式
C([Li])CCC.[CH2:6]([OH:9])[CH2:7][OH:8].Br[CH2:11][CH:12]=[C:13]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[CH3:27])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20]>O>[CH3:27][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=1[C:13]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20])=[CH:12][CH2:11][O:8][CH2:7][CH2:6][OH:9]
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 174Ethylene GlycolHCID 212663063-Bromo-1,1-bis(2-methylphenyl)-1-propeneHCID 178418339Butyllithium

生成物 1

HCID 10517034HCID 10517034、化合物収率 30%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of n-butyllithium in hexanes (14 ml, 2.5 M) was added drop-wise under a nitrogen atmosphere to ethylene glycol (28 ml) at 0° C. When addition was complete the mixture was stirred 0.5 h at room temperature. 3-Bromo-1,1-bis(2-methyl-phenyl)-1-propene (10.5 g, 35 mmol, prepared in a similar way to the method described in Example 26) was added and the reaction mixture was stirred at room temperature for 12 h and at 70° C. for 24 h. Water (100 ml) was added and the mixture was extracted with ethyl acetate (3×100 ml). The combined organic extracts was dried (MgSO4) and the solvent evaporated in vacuo. Flash chromatography of the residue on silica gel (250 g) using a mixture of n-heptane and ethyl acetate (10:1) as eluent provided 3.0 g (30%) of 2-(3, 3-bis(2-methylphenyl)-2-propen-1-yloxy) ethanol.

後処理

  1. additionWhen addition
  2. additionwas added
  3. stirringthe reaction mixture was stirred at room temperature for 12 h and at 70° C. for 24 h
  4. extractionthe mixture was extracted with ethyl acetate (3×100 ml)
  5. dry with materialThe combined organic extracts was dried (MgSO4)
  6. customthe solvent evaporated in vacuo
  7. additiona mixture of n-heptane and ethyl acetate (10:1) as eluent

出典と根拠

ORDレコード
ord-5fe473f3548f4f7d924fa54b22fa6008
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06174898B1

反応ノート

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