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1,3-Dibromopropane → HCID 69663449、化合物

HRID 2212087
ノート
印刷プレビュー

反応式

HRID 2212087 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[CH3:11][O:12][C:13](=[O:25])[CH:14]([S:16]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(=[O:18])=[O:17])[CH3:15].[Br:26][CH2:27][CH2:28][CH2:29]Br>O1CCCC1>[CH3:11][O:12][C:13](=[O:25])[C:14]([S:16]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(=[O:17])=[O:18])([CH3:15])[CH2:29][CH2:28][CH2:27][Br:26]
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 80011,3-DibromopropaneHCID 2733832Lithium hexamethyldisilazaneHCID 109442032-benzenesulfonylpropionic acid methyl ester

生成物 1

HCID 69663449HCID 69663449、化合物収率 16.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran (1M, 6.6 ml, 6.6 mmol) was added dropwise to a stirred solution of 2-benzenesulfonylpropionic acid methyl ester (1.38 g, 5.7 mmol) in tetrahydrofuran at −78° C. The mixture was stirred for 30 min. and 1,3-dibromopropane (3.17 ml, 31.2 mmol) was added. The mixture was slowly warmed to room temperature and stirred for 4 days. After quenching with satd. aqueous NH4Cl, the mixture was extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified on silica gel (i-hexane-ethyl acetate 5–20%) to give the title product (330 mg, 15%).

後処理

  1. stirringstirred for 4 days
  2. customAfter quenching with satd
  3. extractionaqueous NH4Cl, the mixture was extracted into dichloromethane
  4. dry with materialThe combined organic extracts were dried (Na2SO4)
  5. concentrationconcentrated
  6. customThe residue was purified on silica gel (i-hexane-ethyl acetate 5–20%)

出典と根拠

ORDレコード
ord-a46ee2428e86478f8918f6d3a32d7ef2
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07101892B2

反応ノート

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