Reaktion #2715

ord-83e15b83e75e4245842999ea5170336e

Reaktionsgleichung

CC1(C)CC(=O)c2cc(Br)ccc2O1
2,2-dimethyl-6-bromo-chroman-4-one
Cc1cccs1
2-methylthiophene
[Li][CH2]CCC
n-BuLi
CCCCCC
hexane
Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
title compound
Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
2,2-Dimethyl-4(5-methyl-thien-2-yl)-6-bromo-chrom-3-ene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONThis solution was added to a flask
  2. 2
    workup.STIRRINGThe mixture was stirred
  3. 3
    Temperaturto gradually warm to ambient temperature over 8 hours
  4. 4
    workup.STIRRINGstirred for an additional 4 hours at ambient temperature
  5. 5
    Waschenwashed with 10% HCl, brine (20 mL)
  6. 6
    Sonstigedried
  7. 7
    Sonstigethe solvent was removed by evaporation
  8. 8
    SonstigeThe product was purified by chromatography on a silica gel column

Vorschrift

To a cold (-78° C.) solution of 2-methylthiophene (820 mg, 8.3 mmol) in THF (16 mL) was added n-BuLi in hexane (1.6M, 4.4 mL, 8.5 mmol). The mixture was warmed to ambient temperature and stirred for 15 minutes. This solution was added to a flask containing cold (-78° C.) solution of 2,2-dimethyl-6-bromo-chroman-4-one (1.08 g, 4.2 mmol) in THF (4 mL). The mixture was stirred and allowed to gradually warm to ambient temperature over 8 hours, and then stirred for an additional 4 hours at ambient temperature. The mixture was diluted with ethyl acetate (200 mL), washed with 10% HCl, brine (20 mL), dried and the solvent was removed by evaporation. The product was purified by chromatography on a silica gel column to afford the title compound as a colorless off.

Quelle

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