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Borane → 3-(2-Bromophenyl)-1-propanamine

HRID 716947
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 716947
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][C:10]#[N:11].B>O1CCCC1>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH2:10][NH2:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6331BoraneHCID 133082983-(2-Bromophenyl)propanenitrile

Produkt 1

HCID 124139063-(2-Bromophenyl)-1-propanamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Into a 250-mL 3-necked round-bottom flask, was placed a solution of 3-(2-bromophenyl)propanenitrile (2.1 g, 10.00 mmol, 1.00 equiv) in tetrahydrofuran (20 mL). This was followed by the addition of borane (1 mol/L in THF, 50 mL, 5.00 equiv) dropwise with stiffing at 0° C. The resulting solution was stirred for overnight at room temperature. The reaction was then quenched by the addition of 50 mL of water at 0° C. and extracted with 3×50 mL of ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was dissolved in 30 mL of 6N aqueous hydrogen chloride. The aqueous solution was extracted with 30 mL of ethyl acetate and the aqueous layers were combined. The pH value of the aqueous solution was adjusted to 10 with 10% aqueous sodium hydroxide. The resulting solution was extracted with 3×50 mL of ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate, concentrated under vacuum. This resulted in 1.3 g (58%) of 3-(2-bromophenyl)propan-1-amine as colorless oil.

Aufarbeitung

  1. customInto a 250-mL 3-necked round-bottom flask, was placed
  2. customwith stiffing at 0° C
  3. customThe reaction was then quenched by the addition of 50 mL of water at 0° C.
  4. extractionextracted with 3×50 mL of ethyl acetate
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under vacuum
  7. dissolutionThe residue was dissolved in 30 mL of 6N aqueous hydrogen chloride
  8. extractionThe aqueous solution was extracted with 30 mL of ethyl acetate
  9. extractionThe resulting solution was extracted with 3×50 mL of ethyl acetate
  10. dry with materialdried over anhydrous sodium sulfate
  11. concentrationconcentrated under vacuum
  12. customThis resulted in 1.3 g (58%) of 3-(2-bromophenyl)propan-1-amine as colorless oil

Quellen und Nachweise

ORD-Eintrag
ord-79d238cbbba346d49491bc1c478c6888
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09193693B2

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