Reacción #1484

ord-130b3a00a9dc43f5a473799157e45ada

Ecuación de reacción

O=S(Cl)Cl
SOCl2
CC1(C)CCC(=O)c2ccccc21
3,4-dihydro-4,4-dimethylnaphthlen-1(2H)-one
[Li][C](C)(C)C
t-BuLi
CCOCC
ether
CC(=O)c1ccc2c(c1)C(C)(C)CC=C2C(C)(C)C
title compound
CC(=O)c1ccc2c(c1)C(C)(C)CC=C2C(C)(C)C
3,4-Dihydro-4,4-dimethyl-6-acetyl-1-(1,1-dimethylethyl)naphthalene

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaslowly warmed to room temperature
  2. 2
    OtroThe reaction was quenched by addition of saturated NH4Cl
  3. 3
    OtroThe white solids were removed by filtration
  4. 4
    Concentraciónthe clear solution was concentrated to an oil
  5. 5
    Otropurified by column chromatography with ethyl acetate/hexane (1/10)

Procedimiento

To a solution of 6-(2-methyl-1,3-dioxolan-2-yl)!-3,4-dihydro-4,4-dimethylnaphthlen-1(2H)-one ((Compound D15, 353 mg, 1.36 mmol) in 3 ml of dry ether at -78° C. was added dropwise t-BuLi (1 ml, 1.7 mmol, 1.7M solution in pentane). This dear light yellow solution was left at -78° C. for 30 min. Then, fleshly distilled SOCl2 (0.15 ml, 2.0 mmol) was added. The reaction mixture was stirred at -78° C. for additional 30 min and thereafter slowly warmed to room temperature. The reaction was quenched by addition of saturated NH4Cl. The white solids were removed by filtration and the clear solution was concentrated to an oil, and purified by column chromatography with ethyl acetate/hexane (1/10) to give the title compound as a yellow oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723666uspto-grants-1998_03