4-(10-methylundecyl)phenol

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:63.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Next, 363 grams (4.75M) of allyl chloride were added, and mixed with the fluid initial reaction product. The mixture was then heated to 63° C., and exothermed slowly to 73° C. A sample was taken at this point, then acidified and stripped under reduced pressure. TLC revealed the presence on the sample of a small amount of unreacted p-isododecylphenol. mixed with the fluid initial reaction product exothermed slowly to 73° C

Conditions: temp:63.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Next, 363 grams (4.75M) of allyl chloride were added, and mixed with the fluid initial reaction product. The mixture was then heated to 63° C., and exothermed slowly to 73° C. A sample was taken at this point, then acidified and stripped under reduced pressure. TLC revealed the presence on the sample of a small amount of unreacted p-isododecylphenol. mixed with the fluid initial reaction product exothermed slowly to 73° C