2-Ethylhexanoic Acid → HCID 86738319, Verbindung

HRID 2059327

Reaktionsgleichung

Reaktionsgleichung von HRID 2059327
[CH2:1]([Sn:5](Cl)(Cl)Cl)[CH2:2][CH2:3][CH3:4].[OH-].[Na+].[CH2:11]([CH:13]([CH2:17][CH2:18][CH2:19][CH3:20])[C:14]([OH:16])=[O:15])[CH3:12]>O>[CH2:11]([CH:13]([CH2:17][CH2:18][CH2:19][CH3:20])[C:14]([O-:16])=[O:15])[CH3:12].[CH2:1]([Sn+:5])[CH2:2][CH2:3][CH3:4]

Komponenten

5

Versuchsvorschrift

A 500-ml four-necked flask equipped with a stirrer, a thermometer, a dropping funnel and a Liebig condenser is charged with 28.2 g (0.1 mole) of monobutyltin trichloride and 200 ml of deionized water. The contents are warmed to 20°-30° C., and 32 g of a 25% aqueous solution of sodium hydroxide (0.2 mole) is gradually added dropwise. White crystals precipitate out. After the addition, the mixture is stirred at 20°-30° C. for 2 hours. Then, 100 ml of hexane is added, followed by gradual dropwise addition at 20°-30° C. of a separately prepared reaction mixture of 14.4 g (0.1 mole) of 2-ethylhexanoic acid and 4 g (0.1 mole) of sodium hydroxide in 100 ml of water. Care should be taken during the dropping that the flask contents are not made alkaline. After the addition, the mixture is stirred for an hour. The hexane layer is separated and concentrated to give 30 g of monobutyltin mono(2-ethylhexanoate) as a white filmy substance.

Aufarbeitung

  1. customA 500-ml four-necked flask equipped with a stirrer
  2. temperatureThe contents are warmed to 20°-30° C.
  3. customWhite crystals precipitate out
  4. additionAfter the addition
  5. additionThen, 100 ml of hexane is added
  6. additionAfter the addition
  7. stirringthe mixture is stirred for an hour
  8. customThe hexane layer is separated
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-ccdeb90624d7458a813df36b18329442
Quelldatensatz
uspto-grants-1982_03
Patentnummer
US04322519

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