Sulfuric Acid → 2-Amino-3,6-difluorobenzamide

HRID 1467418Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1467418
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].S(=O)(=O)(O)[OH:13].[NH4+].[OH-]>O>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]([NH2:5])=[O:13]

Komponenten

5

Edukt 3

HCID 1118Sulfuric AcidHCID 14923Ammonium Hydroxide2×HCID 450905912-Amino-3,6-difluorobenzonitrile

Produkt 1

HCID 592230322-Amino-3,6-difluorobenzamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

2-Amino-3,6-difluorobenzonitrile (2.3 g, 15 mmol) was added to concentrated sulfuric acid (5 mL) in a 25 mL 2-necked flask equipped with a thermometer with good stirring. The temperature rose to around 40° C. and the mixture became homogeneous. The solution was heated to 70° C. for 2 hours, cooled to room temperature, poured over ice, neutralized with concentrated NH4OH using water and NH4OH to rinse the flask and adding ice as necessary to keep the mixture cold. The separated solid was collected by filtration, washed with water and dried to give 2-amino-3,6-difluorobenzamide, 2.2 g. A second crop of 0.24 g was collected from the cold, concentrated filtrate, 95% overall. M.P. 121-123° C., LC/MS (ESI) m/z 172, 1H NMR (300 MHz, d6-DMSO) δ 7.70 (bs, 1H), 7.63 (bs, 1H), 7.10 (m, 1H), 6.32 (m, 1H), 6.05 (bs, 2H).

Aufarbeitung

  1. customequipped with a thermometer with good stirring
  2. customrose to around 40° C.
  3. temperaturecooled to room temperature
  4. washto rinse the flask
  5. additionadding ice as necessary
  6. filtrationThe separated solid was collected by filtration
  7. washwashed with water
  8. customdried

Quellen und Nachweise

ORD-Eintrag
ord-8068c9cf6a3e43b4a4b8457b2cea027b
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09000162B2

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