Ammonia → 3-(4-(4-Fluorophenoxy)phenyl)propanimidamide

HRID 705841Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 705841
[F:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]#[N:16])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.C(Cl)(C)=O.[NH3:23]>C1(C)C=CC=CC=1.CO>[F:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15](=[NH:23])[NH2:16])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

To a solution of 3-(4-(4-fluorophenoxyl)phenyl)propanenitrile (4.4 g, 18.24 mmol) in toluene (25 mL) and methanol (5.94 mL) was added dropwise AcCl (6.48 mL, 91 mmol) at 0° C. in 5 min. The mixture was stirred at room temperature for 2 h. The mixture was cooled to 0° C. in an ice bath, and ammonia (26.1 mL, 182 mmol) in methanol was added dropwise in 5 min. The mixture was stirred at room temperature overnight. The mixture was filtered to remove the solid, and the solid was washed with toluene (40 mL) and methanol (40 mL). The combined filtrate was concentrated in vacuo, the residue was triturated with diethyl ether, the resulting white solid was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound (5.4 g, 16.12 mmol, 88% yield) as white solid. LCMS: rt=1.03 min, [M+H+]=259

Aufarbeitung

  1. temperatureThe mixture was cooled to 0° C. in an ice bath
  2. stirringThe mixture was stirred at room temperature overnight
  3. filtrationThe mixture was filtered
  4. customto remove the solid
  5. washthe solid was washed with toluene (40 mL) and methanol (40 mL)
  6. concentrationThe combined filtrate was concentrated in vacuo
  7. customthe residue was triturated with diethyl ether
  8. filtrationthe resulting white solid was collected by filtration
  9. washwashed with diethyl ether
  10. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-82a3282461eb4ef2beefb9caf4a49083
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09174968B2

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