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Iodine → 6-Bromohexyl 4-(3-iodophenyl)butyl ether

HRID 2118319
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HRID 2118319 반응식
C([Li])CCC.Br[C:7]1[CH:8]=[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][O:17][C:18]2[C:23]([Br:24])=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:10]=[CH:11][CH:12]=1.[I:25]I.S(=O)(O)[O-].[Na+]>CCCCCC.C1COCC1.O>[I:25][C:7]1[CH:8]=[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][O:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][Br:24])[CH:10]=[CH:11][CH:12]=1
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참가 물질

8

반응물 4

HCID 807IodineHCID 23665763Sodium BisulfiteHCID 691193926-Bromophenyl 4-(3-bromophenyl)butyl etherHCID 178418339Butyllithium

생성물 1

HCID 691198836-Bromohexyl 4-(3-iodophenyl)butyl ether수율 70.8%

시약·촉매·용매 3

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매
2회
HCID 8058Hexane용매

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온도
0 °C

실험 절차

A solution of n-butyl lithium in hexane (1.6 M; 50 ml) was added to a stirred solution of 6-bromophenyl 4-(3-bromophenyl)butyl ether (21 g) in dry THF (150 ml) at −85° C. under nitrogen. After 15 min a solution of iodine (19.8 g) in THF (100 ml) was added dropwise over 20 min. The solution was then allowed to warm up to 0° C. and aqueous sodium bisulphite was added. The mixture was poured into water and extracted into ether. The combined extracts were dried (Na2SO4) and evaporated. The residue was purified by flash silica gel column chromatography (1 kg) eluting with cyclohexane-ether (9:1). The appropriate fractions were evaporated to give the title compound (17 g). LCMS RT=4.41 min.

후처리

  1. extractionextracted into ether
  2. dry with materialThe combined extracts were dried (Na2SO4)
  3. customevaporated
  4. customThe residue was purified by flash silica gel column chromatography (1 kg)
  5. washeluting with cyclohexane-ether (9:1)
  6. customThe appropriate fractions were evaporated

출처 및 근거

ORD 기록
ord-b40e31a4ab1240dcad98430e33960285
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07442839B2

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