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

HRID 2118318
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반응식

HRID 2118318 반응식
[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
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매HCID 962Water용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c16e8c282b58499888fb8b4f7ff19c1b
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07442839B2

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