Reacción #1925195

ord-ca1f668486c64b46a36f0787831754f7

Ecuación de reacción

CO
methanol
CCCCCCCCCCCCCCCCCCO
octadecanol
O=c1[nH]c2ccccc2c(=O)o1
isatoic anhydride
C1CN2CCN1CC2
1,4-diazabicyclo[2.2.2]octane
CCCCCCCCCCCCCCCCCCOC(=O)c1ccccc1N
stearyl anthranilate
Rendimiento 85.0%

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe resultant dark solution was heated to 150° C. for 15 minutes
  2. 2
    TemperaturaThe reaction mixture was then cooled to 50° C.
  3. 3
    workup.ADDITIONwas added
  4. 4
    Filtraciónfollowed by vacuum filtration
  5. 5
    OtroThe solid thus obtained
  6. 6
    Lavadowas washed in the filter funnel with 4×300 milliliter portions of methanol
  7. 7
    Otrowas then dried in air

Procedimiento

A mixture of octadecanol (270 grams, 1.0 mol; obtained from Sigma-Aldrich Co.), isatoic anhydride (244 grams, 1.5 mol; obtained from Sigma-Aldrich Co.), and 1,4-diazabicyclo[2.2.2]octane (56 grams, 0.50 mol; obtained from Sigma-Aldrich Co.), in 1,000 milliliters of dimethylformamide was stirred and heated to 100° C. in a 4 liter beaker. Vigorous gas evolution occurred. After 10 minutes, the resultant dark solution was heated to 150° C. for 15 minutes. The reaction mixture was then cooled to 50° C. and vigorously stirred while 3,000 milliliters of methanol was added. The resultant suspension was stirred for 0.5 hour, followed by vacuum filtration. The solid thus obtained was washed in the filter funnel with 4×300 milliliter portions of methanol and was then dried in air to give the product stearyl anthranilate as white powder (330.5 grams, 85 percent yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06673139B1uspto-grants-2004_01