Reacción #64030

ord-e58c3ee12e4d426cae2ec035c5c58c1e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas elevated up to 80° C
  2. 2
    Lavadothe reaction mixture was washed with water and dilute hydrochloric acid in order
  3. 3
    ExtracciónAfter extraction of the unreacted carboxylic acid with 6% ammonia water
  4. 4
    Secadothe benzene layer was dried over anhydrous sodium sulfate
  5. 5
    Concentraciónconcentrated

Procedimiento

To a solution of 2-carboxymethyl-1,1,4,4,6-pentamethyl-1,2,3,4-tetrahydronaphthalene (30 g; 0.115 mol) in benzene (570 g), lead tetraacetate (66 g; 0.149 mol) and anhydrous lithium chloride (11.5 g; 0.271 mol) were added, and the temperature was elevated up to 80° C. After stirring for 6.5 hours, the reaction mixture was washed with water and dilute hydrochloric acid in order. After extraction of the unreacted carboxylic acid with 6% ammonia water, the benzene layer was dried over anhydrous sodium sulfate and concentrated to give 2-chloromethyl-1,1,4,4,6-pentamethyl-1,2,3,4-tetrahydronaphthalene (18.9 g; 0.075 mol). From the ammonia water layer, there was recovered the unreacted carboxylic acid (9.8 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04767882uspto-grants-1988_08