Menthol → menthyl methacrylate

HRID 1107235Notes

Reaction equation

HRID 1107235 reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH:7]1([CH3:17])[CH2:12][CH2:11][CH:10]([CH:13]([CH3:15])[CH3:14])[CH:9](O)[CH2:8]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[C:1]([O:6][CH:9]1[CH:10]([CH:13]([CH3:15])[CH3:14])[CH2:11][CH2:12][CH:7]([CH3:17])[CH2:8]1)(=[O:5])[C:2]([CH3:4])=[CH2:3]

Participants

5

Conditions

Temperature
150 °C

Procedure

24 g of methacrylic acid, 31 g of menthol and 15 g of p-toluenesulfonic acid dissolved in 500 mL of toluene were heated under reflux at an oil temperature of 150° C. for 19 h. Subsequently, the reaction of the mixed solution was quenched by the addition of salt saturated sodium hydrocarbonate solution. The mixture was extracted with ether, the organic layers were combined and washed with salt saturated sodium bicarbonate solution and then with an aqueous solution of sodium hydroxide, salt saturated ammonium chloride solution, and then dried over salt saturated brine and sodium sulfate anhydous. Finally, the resultant oily product was evaporated under reduced pressure to obtain menthyl methacrylate.

Workup

  1. temperaturewere heated
  2. customSubsequently, the reaction of the mixed solution
  3. customwas quenched by the addition of salt saturated sodium hydrocarbonate solution
  4. extractionThe mixture was extracted with ether
  5. washwashed with salt saturated sodium bicarbonate solution
  6. dry with materialwith an aqueous solution of sodium hydroxide, salt saturated ammonium chloride solution, and then dried over salt saturated brine and sodium sulfate anhydous
  7. customFinally, the resultant oily product was evaporated under reduced pressure

Sources & evidence

ORD record
ord-401fd7c0a10f4754ada2cd6c53496a0f
Source dataset
uspto-grants-2000_05
Patent number
US06060207

Reaction notes

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