Reaktion #2701

ord-bf0cea00f0c14b87bedbeafd627d9061

Reaktionsgleichung

O=C=O
dry-ice
[Li][C](C)(C)C
t-BuLi
CCCCC
pentane
Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)cc1
1-(tol-4-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene
Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)cc1
Compound B
Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)cc1
1-(tol-4-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene
CN(C)C=O
dimethylformamide
Cc1ccc(C2=CCC(C)(C)c3ccc(C=O)cc32)cc1
title compound
Cc1ccc(C2=CCC(C)(C)c3ccc(C=O)cc32)cc1
1-(Tol-4-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehyde

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with water (15 mL)
  2. 2
    TrocknenThe organic layer was dried with MgSO4 and solvent
  3. 3
    Sonstigewas removed under reduced pressure
  4. 4
    SonstigeThe crude material was purified by silicagel chromatography

Vorschrift

To a cold (-78° C.), stirred solution of 1-(tol-4-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene (Compound B 1 g, 3.2 mmol), in THF (17 mL) was added t-BuLi in pentane (1.7M solution, 3 mL, 5.1 mmol). After 10 minutes dry dimethylformamide (DMF) (600 mg, 8 mmol) was added and the dry-ice cooling was replaced with ice-water bath. The mixture was gradually warmed to ambient temperature and diluted with ethylacetate (150 mL), washed with water (15 mL). The organic layer was dried with MgSO4 and solvent was removed under reduced pressure. The crude material was purified by silicagel chromatography to afford the title compound as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728846uspto-grants-1998_03