Propylenediamine → Ammonia

HRID 46163

Reaktionsgleichung

Reaktionsgleichung von HRID 46163
Cl.CO[C:4](=[NH:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[NH2:12][CH2:13][CH:14]([NH2:16])[CH3:15]>CO>[NH3:11].[CH3:15][CH:14]1[CH2:13][NH:12][C:4]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)=[N:16]1

Komponenten

5

Edukt 2

HCID 6567PropylenediamineHCID 5743287Methyl benzimidate hydrochloride

Produkt 2

HCID 222AmmoniaHCID 135889848CID 135889848

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of benzimidic acid methyl ester hydrochloride (1 g) in MeOH (25 ml) was added 1,2-diaminopropane (545 μL) then the mixture was heated to reflux. After 16 h the mixture was cooled to room temperature and concentrated. The residue was taken up in MeOH then passed through Dowex 1×2-400 ion exchange resin (prewashed with 1M NaOH, H2O, MeOH) washing with MeOH. The filtrate was concentrated. Flash column chromatography (gradient, 0-10% MeOH/CHCl3 saturated with NH3) gave 4-methyl-2-phenyl-4,5-dihydro-1H-imidazole as a white solid (1.04 g) which was sufficiently pure for use in the next step. 1H-NMR (400 MHz, CDCl3) δ 7.84 (m, 2 H), 7.55-7.38 (m, 3 H), 4.16 (m, 1 H), 3.95 (dd, J=9.98 and 1.83 Hz, 1 H), 3.40 (m, 1 H), 1.32 (d, J=6.41 Hz, 3 H).

Aufarbeitung

  1. temperaturethe mixture was heated to reflux
  2. concentrationconcentrated
  3. washwashing with MeOH
  4. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-21c609ff16ee4fa194dce5b19780aaa0
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541595B2

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