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Diisopropylamine → Tert-butyl 3-[4,6-Dibromo-2-(2-chlorophenyl)-3-pyridyl]propionate

HRID 1987020
ノート
印刷プレビュー

反応式

HRID 1987020 の反応式
C([Li])CCC.C(NC(C)C)(C)C.[C:13]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])(=[O:15])[CH3:14].[Br:21][C:22]1[CH:27]=[C:26]([Br:28])[N:25]=[C:24]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[Cl:35])[C:23]=1[CH2:36]Br>C1COCC1.C(O)(=O)C>[Br:21][C:22]1[CH:27]=[C:26]([Br:28])[N:25]=[C:24]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[Cl:35])[C:23]=1[CH2:36][CH2:14][C:13]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15]
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

7

反応物 4

HCID 7912DiisopropylamineHCID 10908tert-Butyl acetateHCID 22648203HCID 22648203、化合物HCID 178418339Butyllithium

生成物 1

HCID 57722985Tert-butyl 3-[4,6-Dibromo-2-(2-chlorophenyl)-3-pyridyl]propionate収率 48%

試薬・触媒・溶媒 2

HCID 176Acetic Acid
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-70 °C

実験手順

n-Butyllithium in hexanes (1.6 Molar (hereinafter “M”), 3.75 millilitre (hereinafter “ml”), 6.0 millimole (hereinafter “mmol”)) was added to di-isopropylamine (0.84 ml, 6.0 mmol) in dry THF (15 ml) at −10° under nitrogen. After 5 minutes (hereinafter “min”). the solution was cooled to −70° and tert-butyl acetate (0.5 ml, 3.71 mmol) added dropwise. After stirring at −70° C. for 10 min. under nitrogen, 4,6-Dibromo-3-(bromomethyl)-2-(2-chlorophenyl)pyridine (0.405 grams (hereinafter “g”), 0.92 mmol) in dry THF (15 ml) was added, and the mixture stirred at −70° for 2 h. Glacial acetic acid (2 ml) was added, the temperature allowed to rise to 22° and the solution evaporated in vacuo. The residue was purified by column chromatography over silica (50 g) eluting with cyclohexane-ethyl acetate (9:1)-(5:1) to give the product as an oil (0.21 g).

後処理

  1. temperaturethe solution was cooled to −70°
  2. stirringthe mixture stirred at −70° for 2 h
  3. customto rise to 22°
  4. customthe solution evaporated in vacuo
  5. customThe residue was purified by column chromatography over silica (50 g)
  6. washeluting with cyclohexane-ethyl acetate (9:1)-(5:1)

出典と根拠

ORDレコード
ord-5b2b41687d0645238f9f883becec5880
出典データセット
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07550480B2

反応ノート

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