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Hydrogen Bromide → Dimethyloctylamine hydrobromide

HRID 1110680
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1110680
[BrH:1].[CH3:2][N:3]([CH3:12])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]>O>[BrH:1].[CH3:2][N:3]([CH3:12])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 260Hydrogen BromideHCID 16224Dimethyloctylamine

Produkt 1

HCID 22153594Dimethyloctylamine hydrobromide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Into a 250 ml 3-necked flask equipped with a magnetic stirrer was placed 13.49 g of 48% HBr (0.08 moles) and 60 ml of water. The solution was cooled in an ice bath and dimethyloctylamine (12.58g, 0.08 moles) added dropwise. After the last of the amine had been added (total addition time ca. 30 min) the solution was tested with litmus to assure that it was neutral or acidic, and the water then removed in vacuo. The residue was recrystalized from ethyl acetate and dried under vacuum to give the product, N,N-dimethyl-N-octylamine hydrobromide as a hygroscopic white solid, melting point 156°-158.5 ° C. (yield 14.01 g, 74%).

Aufarbeitung

  1. customInto a 250 ml 3-necked flask equipped with a magnetic stirrer
  2. temperatureThe solution was cooled in an ice bath
  3. addition(total addition time ca. 30 min) the solution
  4. customacidic, and the water then removed in vacuo
  5. customThe residue was recrystalized from ethyl acetate
  6. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-153a6210972a4232a0fd758957484f49
Quelldatensatz
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04976874

Notizen zur Reaktion

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