Pyridine → 2-(Dodecanoyloxy)ethyl benzoate

HRID 2419594Notes

Reaction equation

HRID 2419594 reaction equation
[C:1]([O:9][CH2:10][CH2:11][OH:12])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.N1C=CC=CC=1.[C:19](Cl)(=[O:31])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]>C1C=CC=CC=1>[C:19]([O:12][CH2:11][CH2:10][O:9][C:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:31])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]

Participants

5

Reactant 3

HCID 1049PyridineHCID 8166Dodecanoyl chloride2×HCID 66747Ethylene glycol monobenzoate

Product 1

HCID 203139472-(Dodecanoyloxy)ethyl benzoate

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

To sixteen grams (0.1 mole) of ethylene glycol monobenzoate containing 20 gms (0.25 mole) of pyridine was added 22 gms (0.1 mole) of lauroyl chloride with stirring. With the final addition of lauroyl chloride approximately 50 ml of benzene was added and the mixture stirred for 1 hour. The pyridine hydrochloride was filtered off and the product water washed to remove residual pyridine. The benzene solution was dried over anhydrous sodium sulfate and percolated through a column filled with activated alumina to removal residual free acid. The solvent was removed at reduced pressure. The product, 2-benzoyloxyethyl laurate, was characterized on the basis of the chemical shifts in the NMR spectrum and the absence of OH-stretching and other bands associated with reaction byproducts or impurities.

Workup

  1. additionwas added
  2. stirringthe mixture stirred for 1 hour
  3. filtrationThe pyridine hydrochloride was filtered off
  4. washthe product water washed
  5. customto remove residual pyridine
  6. dry with materialThe benzene solution was dried over anhydrous sodium sulfate
  7. additionfilled with activated alumina to removal residual free acid
  8. customThe solvent was removed at reduced pressure
  9. customother bands associated with reaction byproducts or impurities

Sources & evidence

ORD record
ord-200814f0f9454bc3aaa04035f89a2c8b
Source dataset
uspto-grants-1978_08
Patent number
US04107192

Reaction notes

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