Réaction #6072

ord-48761c7d7d1e44d5995d8941f05c8bb3

Équation de réaction

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
Rendement 90.7%
O=C1OC(=O)C2C(Sc3ccccc3)CC12
2,4-dioxo-6-phenylthio-3-oxabicyclo[3.2.0]heptane
Rendement 90.7%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    LavageThe methylene chloride solution was washed three times with saturated aqueous ammonium chloride solution
  2. 2
    Séchageonce with brine, dried over anhydrous sodium sulfate
  3. 3
    Concentrationconcentrated

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05246931uspto-grants-1993_09