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Hydroxide → 4-Cyclohexyl-1,1-dimethyl-piperazinium hydroxide

HRID 729200
ノート
印刷プレビュー

反応式

HRID 729200 の反応式
[I-].[OH-:2].[CH:3]1([N:9]2[CH2:14][CH2:13][N+:12]([CH3:16])([CH3:15])[CH2:11][CH2:10]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1>O>[OH-:2].[CH:3]1([N:9]2[CH2:10][CH2:11][N+:12]([CH3:16])([CH3:15])[CH2:13][CH2:14]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1
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 961HydroxideHCID 30165Iodide Ion2 回HCID 57610865HCID 57610865、化合物

生成物 1

HCID 670274464-Cyclohexyl-1,1-dimethyl-piperazinium hydroxide

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

The iodide of the cation is exchanged for hydroxide using an ion exchange resin in accordance with the following procedure: 20 g (62 mmol) of the iodide of the cation (R′I) is dissolved in water. 62 g of Dowex SBR resin is added to the solution obtained and it is kept under stirring until the following day. Afterwards, it is filtered, washed with distilled water and a solution of 4-cyclohexyl-1,1-dimethyl-piperazinium hydroxide (R′OH) is obtained which is titrated with HCl (aq.) using phenolphthalein as indicator, obtaining an efficiency in the exchange of higher than 90%. The final solution contains 1 equivalent of hydroxide per 1000 g of solution.

後処理

  1. addition62 g of Dowex SBR resin is added to the solution
  2. customobtained
  3. filtrationAfterwards, it is filtered
  4. washwashed with distilled water

出典と根拠

ORDレコード
ord-918158ed370745239fc456d3d92d1ec7
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07582278B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート