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Piperazine → 1-[2-(Methylsulphonyl)phenyl]piperazine

HRID 1724641
ノート
印刷プレビュー

反応式

HRID 1724641 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([CH3:11])(=[O:10])=[O:9].[NH:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1>>[CH3:11][S:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[N:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)(=[O:10])=[O:9]
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

3

反応物 2

HCID 4837PiperazineHCID 190318Benzene, 1-bromo-2-(methylsulfonyl)-

生成物 1

HCID 112186771-[2-(Methylsulphonyl)phenyl]piperazine収率 34%

反応条件

温度
110 °C

実験手順

A mixture of 2-bromo(methylsulfonyl)benzene (1.10 g, 4.7 mmol) and anhydrous piperazine (2.02 g, 23.5 mmol) was heated at 110° C. overnight. Then, the mixture was cooled and partitioned between 2 N NaOH and CH2Cl2. The separated organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude residue was chromatographed (CHCl3/CH3OH, 9:1, as eluent) to give 8 as a white semisolid (0.36 g, 34% yield). 1H NMR: δ 2.58 (s, 1H, NH, D2O exchanged), 2.84 (s, 4H, piperazinic), 3.14 (s, 3H, CH3), 7.10-7.83 (m, 4H, aromatic).

後処理

temperature
Then, the mixture was cooled
  • custompartitioned between 2 N NaOH and CH2Cl2
  • dry with materialThe separated organic layer was dried over Na2SO4
  • concentrationconcentrated under reduced pressure
  • customThe crude residue was chromatographed (CHCl3/CH3OH, 9:1, as eluent)
  • 出典と根拠

    ORDレコード
    ord-f2fa2b6266a2460a97f9d62d6a21fa0a
    出典データセット
    uspto-grants-2009_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07488730B2

    反応ノート

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