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1-Butanol → 6-Bromohexyl 4-(3-bromophenyl)butyl ether

HRID 2118318
ノート
印刷プレビュー

反応式

HRID 2118318 の反応式
[CH2:1]([OH:5])[CH2:2][CH2:3][CH3:4].Br[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][Br:13].[OH-].[Na+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[Br:13][C:12]1[CH:7]=[C:8]([CH2:4][CH2:3][CH2:2][CH2:1][O:5][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][Br:13])[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

6

反応物 3

HCID 2631-ButanolHCID 123681,6-DibromohexaneHCID 14798Sodium Hydroxide

生成物 1

HCID 218954686-Bromohexyl 4-(3-bromophenyl)butyl ether

試薬・触媒・溶媒 2

HCID 74236Tetrabutylammonium Bromide触媒HCID 962Water溶媒

実験手順

A stirred mixture of 4-3-bromophenyl) butan-1-ol (18 g) (EP 0 995 752A1), 1,6 dibromohexane (48 ml), tetrabutylammonium bromide (1.5 g) and 50% aqueous sodium hydroxide solution (500 ml) was stirred for 2 days at ambient temperature. The mixture was poured into water (1000 ml) and extracted into ethyl acetate. The combined extracts were washed with water, dried (Na2SO4) and evaporated. The residual oil was purified on the biotage eluting with light petroleum (40-60° C.), and then light petroleum (40-60° C.)-ether (9:1). The appropriate fractions were evaporated to give the title compound (18 g) LCMS RT=4.34 min.

後処理

  1. extractionextracted into ethyl acetate
  2. washThe combined extracts were washed with water
  3. dry with materialdried (Na2SO4)
  4. customevaporated
  5. customThe residual oil was purified on the biotage
  6. washeluting with light petroleum (40-60° C.)
  7. customlight petroleum (40-60° C.)-ether (9:1)
  8. customThe appropriate fractions were evaporated

出典と根拠

ORDレコード
ord-c16e8c282b58499888fb8b4f7ff19c1b
出典データセット
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07442839B2

反応ノート

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