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Tetrafluoroboric acid → 5-Bromo-2,4-difluoro-3-methylbenzenediazonium tetrafluoroborate

HRID 330075
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 330075
[Br:1][C:2]1[C:3]([F:11])=[C:4]([CH3:10])[C:5]([F:9])=[C:6]([CH:8]=1)[NH2:7].[N:12]([O-])=O.[Na+].[F:16][B-:17]([F:20])([F:19])[F:18].[H+]>O>[F:16][B-:17]([F:20])([F:19])[F:18].[Br:1][C:2]1[C:3]([F:11])=[C:4]([CH3:10])[C:5]([F:9])=[C:6]([N+:7]#[N:12])[CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 28118Tetrafluoroboric acidHCID 140525645-Bromo-2,4-difluoro-3-methylbenzenamineHCID 23668193Sodium Nitrite

Produkt 1

HCID 140525655-Bromo-2,4-difluoro-3-methylbenzenediazonium tetrafluoroborate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a suspension of 5-bromo-2,4-difluoro-3-methylaniline (24.60 g) in 42% fluoroboric acid (150 ml) with stirring vigorously at -3° to 0° C. was added sodium nitrite (11.47 g) in water (20 ml) dropwise during 40 minutes. After stirring for 1.5 hours at 0° to 5° C., the reacting mixture was cooled with ice bath sufficiently and the resulting precipitate was collected by filtration. This precipitate was washed with small portion of water and ether and dried under reduced pressure to give the title compound (28.83 g) as pale brown prisms, mp 147°-150° C. (decompd.).

Aufarbeitung

  1. stirringAfter stirring for 1.5 hours at 0° to 5° C.
  2. temperaturethe reacting mixture was cooled with ice bath sufficiently
  3. filtrationthe resulting precipitate was collected by filtration
  4. washThis precipitate was washed with small portion of water and ether
  5. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-95d70f47181146238fd762f7ff864139
Quelldatensatz
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04894458

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