4-Cumylphenol → p-Cumylphenyl nicotinate

HRID 2413861Notes

Reaction equation

HRID 2413861 reaction equation
[C:1]([C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)([CH3:3])[CH3:2].Cl.[C:18](Cl)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[N:21][CH:20]=1>N1C=CC=CC=1>[C:18]([O:16][C:13]1[CH:14]=[CH:15][C:10]([C:1]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)([CH3:3])[CH3:2])=[CH:11][CH:12]=1)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[N:21][CH:20]=1

Participants

4

Reactant 2

HCID 117424-CumylphenolHCID 884383-Pyridinecarbonyl chloride, hydrochloride (1:1)

Product 1

HCID 20154093p-Cumylphenyl nicotinate

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Conditions

Temperature
40 °C

Procedure

42.4 g (200 mmol) of p-cumylphenol and 40 g (220 mmol) nicotinic acid chloride hydrochloride was mixed with 600 ml dry pyridine and stirred for 24 hours at 40° C. After cooling precipitated pyridine hydrochloride was sucked off and the filtrate mixed with 150 ml of water. The precipitated raw product was washed with two 100 ml portions of water and recrystallized from methanol.

Workup

  1. temperatureAfter cooling
  2. customprecipitated pyridine hydrochloride
  3. additionthe filtrate mixed with 150 ml of water
  4. customThe precipitated raw product
  5. washwas washed with two 100 ml portions of water
  6. customrecrystallized from methanol

Sources & evidence

ORD record
ord-f9bed4814d744d80899f9704bda89719
Source dataset
uspto-grants-1988_01
Patent number
USRE032581

Reaction notes

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