Hexane → Dimethyl 3-phenylthiocyclobutane-1,2-dicarboxylate

HRID 465768

Reaktionsgleichung

Reaktionsgleichung von HRID 465768
[C:1]([O:9][CH3:10])(=[O:8])/[CH:2]=[CH:3]\[C:4]([O:6][CH3:7])=O.C([S:13]C1C=CC=CC=1)=C.[Cl-].[Cl-].[CH2:22]([Al+2])[CH3:23].[CH3:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]>ClCCCl.C(Cl)Cl>[C:27]1([CH:22]2[CH2:23][CH:3]([C:4]([O:6][CH3:7])=[S:13])[CH:2]2[C:1]([O:9][CH3:10])=[O:8])[CH:26]=[CH:25][CH:30]=[CH:29][CH:28]=1

Komponenten

7

Versuchsvorschrift

To a solution of dimethyl maleate (0.50 mL, 4 mmol) and phenyl vinyl sulfide (0.52 mL, 4 mmol) in 17 mL of 1,2-dichloroethane under nitrogen atmosphere, was added 1 equivalent (4 mL of a 1 M solution in hexane) of ethylaluminum dichloride. The resultant solution was heated at 85° C. for 18 h and then diluted with 75 mL of methylene chloride. The methylene chloride solution was washed three times with saturated aqueous ammonium chloride and once with brine, dried over anhydrous sodium sulfate, filtered and concentrated to give 0.98 g of the title compound; EI-MS, m/e (rel intensity): 280 (M+, 14), 136 (100).

Aufarbeitung

  1. washThe methylene chloride solution was washed three times with saturated aqueous ammonium chloride
  2. dry with materialonce with brine, dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-318cfed1a7c845efb279bf3e11736f46
Quelldatensatz
uspto-grants-1992_10
Patentnummer
US05153352

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