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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Aniline → Formanilide

HRID 1390853
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1390853
NC1C=CC=CC=1.[CH:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9].[K]>CO>[CH:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6115AnilineHCID 86736349Potassium formanilide

Produkt 1

HCID 7671Formanilide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Into a 1-liter Parr autoclave equipped with an agitator, thermowell, rupture disc and cooling coils are placed 84 g. (0.9 mole) of aniline, 16 g. (0.1 mole) of potassium formanilide and 150 g. of methanol. The autoclave is closed and purged with CO. The temperature is raised to 100° C. with atm. steam and CO is introduced at 28 kg/cm2 pressure. Absorption is rapid and little or no heat of reaction is noted. The reaction is run for 31/2 hours, the autoclave cooled to 15° C. and the excess CO vented. The methanol is removed by distillation, xylene added and resulting xylene solution washed with 10 ml. of conc. hydrochloric acid and 200 ml. of water. The organic layer is separated and analyzed by gas-liquid chromatography. The yield of formanilide expected is approximately 93%.

Aufarbeitung

  1. customInto a 1-liter Parr autoclave equipped with an agitator
  2. temperaturethermowell, rupture disc and cooling coils
  3. customThe autoclave is closed
  4. custompurged with CO
  5. additionsteam and CO is introduced at 28 kg/cm2 pressure
  6. customAbsorption
  7. temperaturelittle or no heat of reaction
  8. custom2 hours
  9. temperaturethe autoclave cooled to 15° C.
  10. customThe methanol is removed by distillation, xylene
  11. additionadded
  12. customresulting xylene solution
  13. washwashed with 10 ml
  14. customThe organic layer is separated

Quellen und Nachweise

ORD-Eintrag
ord-6963e4ec0ac247f39f78bdd4c60ac559
Quelldatensatz
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04140716

Notizen zur Reaktion

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