Acetic Acid → 1,3-Bis(1-methylethoxy)-2-propanol

HRID 1050889

Reaktionsgleichung

Reaktionsgleichung von HRID 1050889
[CH:1]([O:4][CH2:5][CH:6]1[CH2:8][O:7]1)([CH3:3])[CH3:2].[CH3:9][CH:10]([CH3:12])[O-:11].[K+].C(O)(=O)C>CCCCCC.C(O)(C)C>[CH:10]([O:11][CH2:8][CH:6]([OH:7])[CH2:5][O:4][CH:1]([CH3:3])[CH3:2])([CH3:12])[CH3:9]

Komponenten

6

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

2-(Isopropoxymethyl)oxirane (23.23 g, 25.1 mL, 200 mmol) was dissolved in hexane (20 mL) and placed in reactor. Separately (1.2 g, 20 mmol) of KH was slowly added to (90.1 g, 115 mL, 1.5 Mol) of isopropanol at RT. After deprotonation was complete the solution of potassium isopropoxide in isopropanol was added to the reactor. All operations were performed in a glove box. The reactor was sealed and heated 80° C. for 24 hours. After cooling acetic acid (20 mmols) and ca. 5 g. of powdered talc were added to the reaction mixture followed by filtration through a plug of celite. The solvent was evaporated and the residue distilled under vacuum affording 20.09 g of 1,3-diisopropoxypropan-2-ol.

Aufarbeitung

  1. customplaced in reactor
  2. additionwas added to the reactor
  3. customAll operations were performed in a glove box
  4. customThe reactor was sealed
  5. filtrationfollowed by filtration through a plug of celite
  6. customThe solvent was evaporated
  7. distillationthe residue distilled under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-058682eadab8481ea18e4183af0407f7
Quelldatensatz
uspto-grants-2016_07
Patentnummer
US09388106B2

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