Reacción #52849

ord-60e46af075ba419ea97873f93ff81cab

Ecuación de reacción

CC1(C)CCC(=O)c2cc(Br)ccc21
4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1-one
CC1(C)CCC(=O)c2cc(Br)ccc21
Compound G
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1-one
C1CCOC1
THF
Sc1ccccc1
thiophenol
CCN(CC)CC
triethylamine
C1CCOC1
THF
CC1(C)CC=C(Sc2ccccc2)c2cc(Br)ccc21
title compound
CC1(C)CC=C(Sc2ccccc2)c2cc(Br)ccc21
4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with ether (3×50 mL)
  2. 2
    LavadoThe combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL)
  3. 3
    SecadoThe organic layer was dried (MgSO4)
  4. 4
    workup.DISTILLATIONthe solvent distilled off at reduced pressure

Procedimiento

To a stirred solution of 4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one (Compound G, 1.48 g, 5.9 mmol), titanium tetrachloride (1.09 g, 5.7 mmol) and THF (10 mL) was added a mixture of thiophenol (660 mg, 6 mmol), triethylamine (1.16 g, 11.5 mmol) and THF (20 mL) via an addition funnel at ambient temperature. The mixture was stirred for 5 h, and water (10 mL) was added, extracted with ether (3×50 mL). The combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried (MgSO4) and the solvent distilled off at reduced pressure. After silicagel chromatography the title compound was obtained as a colorless oil

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06855832B2uspto-grants-2005_02