Reacción #1322

ord-445de8cff1a04382843fe36a0a03ecd1

Ecuación de reacción

C#Cc1ccc2c(c1)C(C)(C)CCC2=O
6-ethynyl-1,2,3,4-tetrahydro-4,4-dimethylnaphthalen-1-one
C#Cc1ccc2c(c1)C(C)(C)CCC2=O
6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
C#Cc1ccc2c(c1)C(C)(C)CCC2=O
Compound K
C#Cc1ccc2c(c1)C(C)(C)CCC2=O
6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
CCOC(=O)c1ccc(I)cc1
ethyl 4-iodobenzoate
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3=O)cc1
title compound
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3=O)cc1
Ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solution mixture was flushed with argon for 5 minutes
  2. 2
    FiltraciónThe reaction mixture was filtered through celite
  3. 3
    Concentraciónthe filtrate concentrated in vacuo
  4. 4
    OtroPurification by flash chromatography (silica, 10% EtOAc-hexane)

Procedimiento

To a solution of 8.8 g (47.8 mmol) of 6-ethynyl-1,2,3,4-tetrahydro-4,4-dimethylnaphthalen-1-one (Compound K) flushed for 15 minutes with a stream of argon, and 13.2 g (47.8 mmol) of ethyl 4-iodobenzoate in 200 ml of triethylamine was added 1.1 g (1.6 mmol) of bis(triphenylphosphine)palladium(II) chloride and 0.30 g (1.6 mmol) of cuprous iodide. The solution mixture was flushed with argon for 5 minutes and then stirred at ambient temperature for 18 hours. The reaction mixture was filtered through celite and the filtrate concentrated in vacuo. Purification by flash chromatography (silica, 10% EtOAc-hexane) yielded the title compound as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723620uspto-grants-1998_03