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Stannous Chloride → 5-Bromo-2-cyclopropylaniline

HRID 339472
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 339472
[Sn](Cl)Cl.[Br:4][C:5]1[CH:6]=[CH:7][C:8]([CH:14]2[CH2:16][CH2:15]2)=[C:9]([N+:11]([O-])=O)[CH:10]=1>C(O)C.O>[Br:4][C:5]1[CH:6]=[CH:7][C:8]([CH:14]2[CH2:16][CH2:15]2)=[C:9]([CH:10]=1)[NH2:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 24479Stannous Chloride2×HCID 6713434-Bromo-1-cyclopropyl-2-nitrobenzene

Produkt 1

HCID 47122485-Bromo-2-cyclopropylaniline

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

Tin (II) chloride (16.0 g, 0.10 mol) is added in one portion to a solution of crude 5-bromo-2-cyclopropylnitrobenzene (8.68 g) in ethanol (190 ml) and water (1.9 ml). The reaction mixture is stirred at room temperature overnight, followed by addition of further tin (II) chloride (28 g, 0.175 mol) and additional stirring overnight. After concentration in vacuo ice is added, and the solution is basified with 2M aqueous sodium hydroxide. After extraction with ethyl acetate (×2) the organic phase is washed again with 2M aqueous sodium hydroxide, then also distilled water and brine. After drying over magnesium sulfate the solution is concentrated in vcauo to give a brown oil which is purified by flash column chromatography on silica gel (9:1 isohexane/ethyl acetate eluant) to afford 5-bromo-2-cyclopropylaniline as a brown oil.

Aufarbeitung

  1. stirringadditional stirring overnight
  2. concentrationAfter concentration in vacuo ice
  3. additionis added
  4. extractionAfter extraction with ethyl acetate (×2) the organic phase
  5. washis washed again with 2M aqueous sodium hydroxide
  6. dry with materialAfter drying over magnesium sulfate the solution
  7. concentrationis concentrated in vcauo
  8. customto give a brown oil which
  9. customis purified by flash column chromatography on silica gel (9:1 isohexane/ethyl acetate eluant)

Quellen und Nachweise

ORD-Eintrag
ord-f0c62ef52de1426aabf80164a404c482
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08895474B2

Notizen zur Reaktion

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