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HRID 132974Erstellt: 24. Oktober 2026

2-Amino-1-butanol → 1,3-Bis[(4-ethyl-4,5,-dihydro-2-oxazolyl)methyl]benzene

https://huagongshe.com/de/reaction/132974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-1-butanolHCID 22129—
Edukt1,3-BenzenediacetonitrileHCID 69375—
KatalysatorCadmium nitrate tetrahydrateHCID 56924536—
LösungsmittelO-XyleneHCID 7237—
Produkt1,3-Bis[(4-ethyl-4,5,-dihydro-2-oxazolyl)methyl]benzeneHCID 5881071667%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

In a one liter four-necked round-bottom flask equipped with a condenser, N2 inlet/outlet, magnetic stirrer, and thermometer, was charged with 52.65 g of 1,3-phenylene-diacetonitrile (0.337 mol, Aldrich), 78.13 g of 2-amino-1-butanol (0.876 mol, Aldrich), and 3.38 g of cadmium nitrate tetrahydrate (0.011 mol, Aldrich) in 300 mL of o-xylene. The mixture was heated to 130° C. and the reaction was run for 72 hours. The cooled mixture was washed with de-ionized water (2×200 mL). The organic layer was dried over sodium sulfate and acidic alumina gel. After removal of solvent in vacuo, 67.21 g of an amber liquid resin was obtained in a yield of 67%. The viscosity of this resin at room temperature is 250 mPa.·. 1H NMR (CDCl3, 400 MHz): δ 7.11-7.19 (m, 4H), 4.20 (t, 2H), 3.91-3.97 (m, 2H), 3.77 (t, 2H), 3.52 (s, 4H), 1.53-1.61 (m, 2H), 1.40-1.47 (m, 2H), 0.86 (t, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390430B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-fb9b9f551bd34ee5a3477b6d658efbf8
Quellennotizuspto-grants-2008_06