o-Cyclohexylphenol → 3-Pyridinecarboxylic acid, 2-cyclohexylphenyl ester, hydrochloride

HRID 2413858

Reaktionsgleichung

Reaktionsgleichung von HRID 2413858
[CH:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[OH:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.[C:15]([Cl:23])(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=1>N1C=CC=CC=1>[ClH:23].[C:15]([O:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1)(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
30 °C

Versuchsvorschrift

15 g (85 mmol) of o-cyclohexylphenol and 16.5 g (93 mmol) of nicotinic acid chloride hydrochloride was mixed with 200 ml of dry pyridine and stirred for 24 hours at 30° C. After cooling precipitated pyridine hydrochloride was sucked off and 300 ml of water added. The precipitated raw product was washed with two 200 ml portions of water, dissolved in alcohol and reduced by means of a rotary evaporator. The remaining viscous oil was dissolved in 500 ml of dry ether and hydrochlorinated with HCl gas. Subsequently, the mixture was filtered, washed with ether and dried.

Aufarbeitung

  1. temperatureAfter cooling
  2. customprecipitated pyridine hydrochloride
  3. addition300 ml of water added
  4. customThe precipitated raw product
  5. washwas washed with two 200 ml portions of water
  6. dissolutiondissolved in alcohol
  7. customreduced by means of a rotary evaporator
  8. dissolutionThe remaining viscous oil was dissolved in 500 ml of dry ether and hydrochlorinated with HCl gas
  9. filtrationSubsequently, the mixture was filtered
  10. washwashed with ether
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-af0c31276892453c901c210bb3fab831
Quelldatensatz
uspto-grants-1988_01
Patentnummer
USRE032581

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