Reaktion #167118

ord-7e09ee270ba2465f88cc80618bdc441c

Reaktionsgleichung

CC(=O)C1=CC2SC=CC2S1
1-(3a,6a-Dihydro-thieno[3,2-b]thiophen-2-yl)-ethanone
C[N+](C)(C)c1ccccc1.C[N+](C)(C)c1ccccc1.C[N+](C)(C)c1ccccc1.[Br-].[Br-].[Br-]
phenyltrimethylammonium tribromide
O=C(CBr)C1=CC2SC=CC2S1
title compound
O=C(CBr)C1=CC2SC=CC2S1
2-Bromo-1-(3a,6a-dihydro-thieno[3,2-b]thiophen-2-yl)-ethanone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe suspension was filtered over CELITE
  2. 2
    workup.ADDITIONThe filtrate was diluted with diethyl ether
  3. 3
    Waschenwashed with saturated aqueous NaHCO3 and brine
  4. 4
    Trocknenthen dried over MgSO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated

Vorschrift

1-(3a,6a-Dihydro-thieno[3,2-b]thiophen-2-yl)-ethanone (453 mg, 2.48 mmol) was dissolved in THF (12 mL) and phenyltrimethylammonium tribromide (932 mg, 2.48 mmol) was added. After stirring for 1 h, the suspension was filtered over CELITE. The filtrate was diluted with diethyl ether, then washed with saturated aqueous NaHCO3 and brine then dried over MgSO4, filtered and concentrated to afford the title compound which was carried on without purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08841278B2uspto-grants-2014_09