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

HRID 2118319
ノート
印刷プレビュー

反応式

HRID 2118319 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒
2 回
HCID 8058Hexane溶媒

反応条件

温度
0 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-b40e31a4ab1240dcad98430e33960285
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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