Water → 4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)aniline

HRID 704469

Reaktionsgleichung

Reaktionsgleichung von HRID 704469
O.[Cl:2][C:3]1[C:8]([O:9][CH2:10][C:11]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[O:12])=[CH:7][C:6]([N+:19]([O-])=O)=[C:5]([F:22])[CH:4]=1>C(O)(=O)C.[Fe]>[Cl:2][C:3]1[C:8]([O:9][CH2:10][C:11]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[O:12])=[CH:7][C:6]([NH2:19])=[C:5]([F:22])[CH:4]=1

Komponenten

5

Edukt 2

HCID 962WaterHCID 146178494-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene

Produkt 1

HCID 146178504-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)anilineAusbeute 75,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23925IronKatalysatorHCID 176Acetic AcidLösungsmittel2×

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of iron powder (115 g), acetic acid (29 g) and water (551 g) was heated at 80° C., and a solution of the compound (III) (132 g) in acetic acid (200 g) was dropwise added thereto in 1 hour, followed by heating under reflux for 5 hours. The reaction mixture was filtered to remove insoluble materials, and the filtrate was extracted with ethyl acetate. The extract was concentrated under reduced pressure. The residue was distilled off under reduced pressure to give 4-chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)aniline (Compound (II)) (90 g). Yield, 75 b.p., 145°-149° C./0.4 mmHg. m.p., 32°-3420 C.

Aufarbeitung

  1. temperatureby heating
  2. temperatureunder reflux for 5 hours
  3. filtrationThe reaction mixture was filtered
  4. customto remove insoluble materials
  5. extractionthe filtrate was extracted with ethyl acetate
  6. concentrationThe extract was concentrated under reduced pressure
  7. distillationThe residue was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-fa61744c7add4522ab5fde25b4ef6dac
Quelldatensatz
uspto-grants-1991_01
Patentnummer
US04987247

Verknüpfte Notizen

Wird geladen…