Water → 4-(2-Hydroxyethyl)cyclohexan-1-ol

HRID 40982

Reaktionsgleichung

Reaktionsgleichung von HRID 40982
[OH:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][C:7](=[O:10])[CH2:6][CH2:5]1.[AlH4-].[Li+].O.[OH-].[Na+]>CCOCC.C1COCC1>[OH:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][CH:7]([OH:10])[CH2:6][CH2:5]1

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

4-(2-Hydroxyethyl)cyclohexanone (2.00 g, 0.0141 mol) was dissolved in ether (30.00 mL) and was cooled at 0° C. To the reaction was added 1.0 M lithium tetrahydroaluminate in ether (14.1 mL) and the resulting mixture was stirred at 0° C. for 2 hours and at 25° C. for 16 hours. To the reaction was added THF (20.00 mL) and this mixture was cooled at 0° C. and then water (0.40 mL, 0.022 mol) was added, followed by 1.00 M sodium hydroxide (0.40 mL). To the reaction was then added ether (100.00 mL) and the resulting mixture was stirred for 10 minutes, then was filtered and the filtrate was concentrated using a rotary evaporator to provide the crude product. The crude product was used in the next reaction without further purification.

Aufarbeitung

  1. temperaturethis mixture was cooled at 0° C.
  2. filtrationwas filtered
  3. concentrationthe filtrate was concentrated
  4. customa rotary evaporator

Quellen und Nachweise

ORD-Eintrag
ord-80fda129872c4577b0185fdb7b5229dc
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08530485B2

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