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Trimethyl Phosphate → HCID 86608378、化合物

HRID 1821105
ノート
印刷プレビュー

反応式

HRID 1821105 の反応式
[CH2:1]([N:3]([CH2:10][CH3:11])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH3:2].[CH3:12][O:13][P:14](=[O:19])([O:17]C)[O:15]C>CO>[P:14]([O-:19])([O-:17])([O-:15])=[O:13].[CH2:10]([N+:3]([CH2:1][CH3:2])([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH3:12])[CH3:11].[CH2:10]([N+:3]([CH3:12])([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH2:1][CH3:2])[CH3:11].[CH2:10]([N+:3]([CH3:12])([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH2:1][CH3:2])[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10541Trimethyl PhosphateHCID 524224N,N-diethylhexylamine

生成物 1

HCID 86608378HCID 86608378、化合物収率 134.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a 200 ml four necked flask equipped with a stirrer, a dropping funnel, a cooling tube and a thermometer, 78.65 g (0.5 mol) of diethyl hexyl amine and 50 ml of methanol were charged and heated, to which 70.04 g (0.50 mol) of trimethyl phosphoric acid was dropped slowly taking one hour or more and refluxed for 15 hours. After reaction, they were cooled to room temperature and 136.80 g of diethyl hexyl methyl ammonium phosphate was obtained by drying under a reduced pressure. Then, 136.80 g of the obtained diethyl hexyl methyl ammonium phosphate was dissolved in 50 ml of water, and a solution in which 189.66 g of lithium bis(pentafluoroethane sulfonyl) imide was dissolved in 50 ml of water was added thereto at a room temperature and stirred. From separated two layers, the lower layer was fractionated and by-products were removed by adding 40 wt % of purified water and water washing five times, and vacuum drying was applied to obtain 262.43 g of diethyl hexyl methyl ammonium bis(trifluoromethane sulfonyl) imide. As a result of ICP analysis, the total alkali metals was 2.4 ppm or less, chloride ion was 0.6 ppm, and each of iodide and bromide ions was 0.1 ppm or less (lower than ICP detection limit).

後処理

  1. additionwas dropped slowly
  2. waittaking one hour or more
  3. temperaturerefluxed for 15 hours
  4. customAfter reaction, they

出典と根拠

ORDレコード
ord-95751424b780498ba3dc3c06d254ac50
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07605271B2

反応ノート

読み込み中…

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