2-Fluoro-6-nitroaniline → 2-Fluoro-6-nitrophenylthiocyanate

HRID 514829Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 514829
[F:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[C:3]=1N.N([O-])=O.[Na+].[S-:16][C:17]#[N:18].[K+]>S(=O)(=O)(O)O.O>[F:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[C:3]=1[S:16][C:17]#[N:18]

Komponenten

6

Edukt 3

HCID 873162-Fluoro-6-nitroanilineHCID 516872Potassium thiocyanateHCID 23668193Sodium Nitrite

Produkt 1

HCID 904190222-Fluoro-6-nitrophenylthiocyanateAusbeute 99,9 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel3×HCID 1118Sulfuric AcidLösungsmittel

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

A solution of 2-fluoro-6-nitroaniline (3 g, 0.02 mol) in conc. sulphuric acid (30 mL) and water (30 mL) was diazotized at 0-3° C. for 90 min with aqueous sodium nitrite (1.45 g, 0.021 mol). After addition of potassium thiocyanate (2.522 g, 0.026 mol) in water (10 mL), the diazo-liquor was stirred vigorously into a suspension of cuprous thiocyanate (6.05 g, 0.05 mol) in water (20 mL) at 5° C. After stirring at 5° C. for 2 hr, the mixture was then heated at 70° C. for 20 min, then was cooled overnight, filtered, and the cake extracted with EtOAc to get the crude product (3.96 g) which was used in the next step without further purification. LC-MS: m/z 199.2 (M+H)+

Aufarbeitung

  1. temperaturethe mixture was then heated at 70° C. for 20 min
  2. temperaturewas cooled overnight
  3. filtrationfiltered
  4. extractionthe cake extracted with EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-522fe75e085945588571e3fc32547aab
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09108921B2

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