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Methylamine → (3-Methoxy)-alpha-methyl-alpha-[(methylamino)methyl]benzene methanol

HRID 2198883
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2198883
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2([CH3:12])[CH2:11][O:10]2)[CH:6]=[CH:7][CH:8]=1.[CH3:13][NH2:14]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:12])([CH2:11][NH:14][CH3:13])[OH:10])[CH:6]=[CH:7][CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 6329Methylamine2×HCID 204969162-(3-Methoxyphenyl)-2-methyloxirane

Produkt 1

HCID 62773765(3-Methoxy)-alpha-methyl-alpha-[(methylamino)methyl]benzene methanol

Versuchsvorschrift

2-(3-Methoxyphenyl)-2-methyloxiran (34.0 g) was stirred with aqueous methylamine (100 ml, 33%) and alcoholic methylamine (200 ml, 33%) overnight at ambient temperature. The mixture was evaporated to an oil under reduced pressure, dissolved in hydrochloric acid (2 M) and extracted with toluene. After basifying the aqueous acid with sodium hydroxide (5 M) the basic oil was extracted with toluene and dried (MgSO4). The solvent was removed under reduced pressure to leave the title compound as an oil (27.7 g). The hydrochloride was formed in isopropyl alcohol-ethereal hydrogen chloride, m.p. 155°-156° C. (Found: C, 57.55; H, 8.3; N, 5.8% C11H17NO2HCl requires C, 57.0; H, 7.8; N, 6.0%.

Aufarbeitung

  • customThe mixture was evaporated to an oil under reduced pressure
  • dissolutiondissolved in hydrochloric acid (2 M)
  • extractionextracted with toluene
  • extractionwas extracted with toluene
  • dry with materialdried (MgSO4)
  • customThe solvent was removed under reduced pressure
  • Quellen und Nachweise

    ORD-Eintrag
    ord-51f1fa9dfe4c4beaa34acf22188b01d7
    Quelldatensatz
    uspto-grants-1982_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04360519

    Notizen zur Reaktion

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