반응 #1484

ord-130b3a00a9dc43f5a473799157e45ada

반응 방정식

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

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723666uspto-grants-1998_03