Reaktion #552951

ord-4428d5b6560c4e069945e042110f6c04

Reaktionsgleichung

O=C1C=CC(=O)O1
maleic anhydride
C=CSc1ccccc1
phenyl vinyl sulfide
C[CH2][Al+2].[Cl-].[Cl-]
ethylaluminum dichloride
O=C1OC(=O)C2C(Sc3ccccc3)CC12
title compound
Ausbeute 90.7%
O=C1OC(=O)C2C(Sc3ccccc3)CC12
2,4-dioxo-6-phenylthio-3-oxabicyclo[3.2.0]heptane
Ausbeute 90.7%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe methylene chloride solution was washed three times with saturated aqueous ammonium chloride solution
  2. 2
    Trocknenonce with brine, dried over anhydrous sodium sulfate
  3. 3
    Einengenconcentrated

Vorschrift

To a solution of maleic anhydride (0.39 g, 4 mmol) and phenyl vinyl sulfide (0.52, 4 mmol) in 17 mL of 1,2-dichloroethane under nitrogen, was added 2 mL (0.5 equiv) of ethylaluminum dichloride. The resultant solution was stirred at ambient temperature for 0.5 h and then diluted with 75 mL of methylene chloride. The methylene chloride solution was washed three times with saturated aqueous ammonium chloride solution and once with brine, dried over anhydrous sodium sulfate and concentrated to give 0.85 g of the title compound; EI-MS, m/e (rel intensity): 234 (M+, 23), 136 (100), 109 (12), 91 (21).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05153352uspto-grants-1992_10