1,3-Dibromopropane → (3-Bromo-propyl)-(2-chloro4,6-dimethyl-phenyl)-amine

HRID 1246303

Reaktionsgleichung

Reaktionsgleichung von HRID 1246303
[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([CH3:10])[C:3]=1[NH2:4].C([Li])CCC.[Br:16][CH2:17][CH2:18][CH2:19]Br>O1CCOCC1>[Br:16][CH2:17][CH2:18][CH2:19][NH:4][C:3]1[C:5]([CH3:10])=[CH:6][C:7]([CH3:9])=[CH:8][C:2]=1[Cl:1]

Komponenten

5

Edukt 3

HCID 80011,3-DibromopropaneHCID 1130332-Chloro-4,6-dimethylanilineHCID 178418339Butyllithium

Produkt 1

HCID 21916144(3-Bromo-propyl)-(2-chloro4,6-dimethyl-phenyl)-amineAusbeute 67,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

To a solution of the 2-chloro-4,6-dimethyl aniline (16.9 g g, 108 mmol) in 1,4-dioxane (80 mL) was added n-butyl lithium solution (2.5 M in hexanes, 48 mL), dropwise, at 0° C. under argon. The reaction mixture was warmed up to rt and stirred for 20 min. 1,3-Dibromopropane (109 g, 543 mmol) was added and the reaction mixture was stirred overnight. The mixture was filtered through celite and concentrated. Purification was carried out by reverse phase chromatography using water, methanol and trifluoroacetic acid to obtain product (20.01 g, 72.5 mmol, 67%) as brown oil. LC/MS: tR=1.5 min. [M+H] 277. 1H NMR (CD3OD) δ: 7.12 (s, 1H), 6.99 (s, 1H), 3.52 (t, J=6.65 Hz, 2H), 3.36 (t, J=6.75 Hz, 2H), 2.36 (s, 3H), 2.29 (s, 3H), 2.14 (m, 2H).

Aufarbeitung

  1. customat 0° C.
  2. stirringthe reaction mixture was stirred overnight
  3. filtrationThe mixture was filtered through celite and
  4. concentrationconcentrated
  5. customPurification

Quellen und Nachweise

ORD-Eintrag
ord-ae5ebf9444f24fcbbdd77cd55a77b0e3
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07125990B2

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