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Stannous chloride dihydrate → 3-Chloro-4-ethylaniline

HRID 1781051
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1781051
[Cl:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9].O.O.Cl[Sn]Cl>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9])[NH2:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 61436Stannous chloride dihydrateHCID 41134491-Chloro-2-ethyl-5-nitrobenzene

Produkt 1

HCID 211899483-Chloro-4-ethylanilineAusbeute 98 %

Versuchsvorschrift

A solution of 8.9 g (48 mmol) of 31 and 54.6 g (241 mmol) of SnCl2.2H2O in 100 mL of absolute alcohol was refluxed for 1 h. It was evaporated to remove most of the solvent and the residue was treated with 2N NaOH to pH=9. The mixture was filtered and the solid was washed with methanol (10 mL) and ethyl acetate (200 mL). The filtrate was separated and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic solution was dried (MgSO4) and evaporated to leave 7.31 g (98%) of liquid. 1H NMR (CDCl3), 1.178 (t, 3, J=7.5), 2.639 (q, 2, J=7.4), 6.532 (dd, 1, J=2.2, 8.1), 6.700 (d, 1, J=2.2), 6.996 (d, 1, J=8.2).

Aufarbeitung

  1. customIt was evaporated
custom
to remove most of the solvent
  • additionthe residue was treated with 2N NaOH to pH=9
  • filtrationThe mixture was filtered
  • washthe solid was washed with methanol (10 mL) and ethyl acetate (200 mL)
  • customThe filtrate was separated
  • extractionthe aqueous phase was extracted with ethyl acetate (2×50 mL)
  • dry with materialThe combined organic solution was dried (MgSO4)
  • customevaporated
  • Quellen und Nachweise

    ORD-Eintrag
    ord-1f41145c35d14389a62208c891c594b4
    Quelldatensatz
    uspto-grants-1997_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US05631373

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