Isopropanol → Dodecyl propan-2-yl hydrogen phosphate

HRID 441369ノート

反応式

HRID 441369 の反応式
[CH2:1]([OH:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH:14]([OH:17])([CH3:16])[CH3:15].[O:18]=[P:19]12OP3(OP(OP(O3)(O1)=O)(=O)[O:20]2)=O>CCCCCC>[P:19]([OH:20])([O:17][CH:14]([CH3:16])[CH3:15])([O:13][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])=[O:18]

参加物

5

実験手順

Dodecyl isopropyl hydrogen phosphate was prepared by slowly adding a mixture of 0.2 g. mole each of 1-dodecanol and isopropyl alcohol to a stirred slurry of 0.1 g. mole of P2O5 in 100 ml. hexane, holding the temperature of the reaction mixture below its boiling point by use of a water bath. After the addition was complete, stirring was continued until the mixture was clear and then the hexane was distilled off, the last portion under reduced pressure. The product was a clear, colorless liquid which crystallized slowly into a waxy, white solid. It was primarily the desired mixed ester with small amounts of the two symmetrical diesters.

後処理

  1. additionby slowly adding
  2. additiona mixture of 0.2 g
  3. additionAfter the addition
  4. distillationthe hexane was distilled off
  5. customcrystallized slowly into a waxy, white solid
  6. additiondesired mixed ester with small amounts of the two symmetrical diesters

出典と根拠

ORDレコード
ord-83a3f0591fb845038b09d208a5907148
出典データセット
uspto-grants-1977_08
特許番号
US04039636

反応ノート

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