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Isopropylamine → 4-(4-methoxyphenyl)-N-(1-methylethyl)butylamine

HRID 2417991
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2417991
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12]Br)=[CH:5][CH:4]=1.[CH:14]([NH2:17])([CH3:16])[CH3:15]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][NH:17][CH:14]([CH3:16])[CH3:15])=[CH:5][CH:4]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 6363IsopropylamineHCID 5781911-(4-Bromobutyl)-4-methoxybenzene

Produkt 1

HCID 204469294-(4-methoxyphenyl)-N-(1-methylethyl)butylamine

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A solution of (50 ml) isopropylamine and 4-(4-methoxyphenyl)butyl bromide (13.7 g) in a glass lined vessel was heated under nitrogen (initial pressure, 500 psi) for 12 hours at 100° C. The solvent was removed in vacuo and water (200 ml) was added to the residue. The solution was acidified with concentrated hydrochloric acid and the solution was extracted with ether. The extract was dried over potassium carbonate and the solvent was removed in vacuo. The residue, 4-(4-methoxyphenyl)-N-(1-methylethyl)butylamine, weighed 9.3 g (75%). The identity and purity (94.8%) of the product was determined by mass spectrum and gas chromatography.

Aufarbeitung

  1. customThe solvent was removed in vacuo and water (200 ml)
  2. additionwas added to the residue
  3. extractionthe solution was extracted with ether
  4. dry with materialThe extract was dried over potassium carbonate
  5. customthe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-70a8b85604b7449ebbe788cd8acdafb8
Quelldatensatz
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04471116

Notizen zur Reaktion

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