Reacción #2710

ord-1e1b81ee8df24843ab572b0af6fcff4f

Ecuación de reacción

CC1(C)CC(=O)c2cc(Br)ccc2S1
2,2-dimethyl-6-bromo-thiochroman-4-one
CC1(C)CC(=O)c2cc(Br)ccc2S1
Compound M
CC1(C)CC(=O)c2cc(Br)ccc2S1
2,2-dimethyl-6-bromo-thiochroman-4-one
Cc1ccc(S(=O)(=O)O)cc1
pTSA
Cc1ccc(Br)cc1
4-bromotoluene
[Li][C](C)(C)C
t-BuLi
CCCCC
pentane
Cc1ccc(C2=CC(C)(C)Sc3ccc(Br)cc32)cc1
title compound
Cc1ccc(C2=CC(C)(C)Sc3ccc(Br)cc32)cc1
2,2-Dimethyl-4(tol-4-yl)-6-bromo-thiochrom-3-ene

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThis mixture was added to a flask
  2. 2
    workup.STIRRINGand stirred for 16 hours at ambient temperature
  3. 3
    OtroThe reaction was quenched
  4. 4
    workup.ADDITIONby adding aq. NH4Cl
  5. 5
    Extracciónthe resulting mixture was extracted with ethylacetate
  6. 6
    Lavadowashed with brine
  7. 7
    Otrodried
  8. 8
    Otrothe solvent was removed by evaporation
  9. 9
    OtroThe product was isolated by chromatography on silica gel
  10. 10
    Temperaturaheated to 50° C. for 3 hours
  11. 11
    Lavadowashed with 10% NaHCO3 (5 mL), brine (5 mL)
  12. 12
    Secadodried with MgSO4
  13. 13
    Otrothe solvent was removed by evaporation

Procedimiento

To a cold (-78° C.) solution of 4-bromotoluene (720 mg, 4.2 mmol) in THF (8 mL) was added t-BuLi in pentane (1.7M, 0.5 mL, 0.85 mmol). The mixture was warmed to ambient temperature over 30 minutes with stirring. This mixture was added to a flask containing 2,2-dimethyl-6-bromo-thiochroman-4-one (Compound M, 140 mg, 0.4 mmol) and THF (2 mL). and stirred for 16 hours at ambient temperature. The reaction was quenched by adding aq. NH4Cl, and the resulting mixture was extracted with ethylacetate, washed with brine, dried and the solvent was removed by evaporation. The product was isolated by chromatography on silica gel. The material was dissolved in dichloromethane (5 mL) and pTSA (5 mg) was added and heated to 50° C. for 3 hours. The misture was diluted with ethylacetate (20 mL), washed with 10% NaHCO3 (5 mL), brine (5 mL), dried with MgSO4 and the solvent was removed by evaporation to afford the title compound as an off.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728846uspto-grants-1998_03