Tetrafluoroboric acid → 2,3-Dichloro-4,5-difluorobenzenediazonium tetrafluoroborate

HRID 414376Notes

Reaction equation

HRID 414376 reaction equation
[Cl:1][C:2]1[C:8]([Cl:9])=[C:7]([F:10])[C:6]([F:11])=[CH:5][C:3]=1[NH2:4].[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].[Cl:1][C:2]1[C:8]([Cl:9])=[C:7]([F:10])[C:6]([F:11])=[CH:5][C:3]=1[N+:4]#[N:12]

Participants

5

Reactant 3

HCID 28118Tetrafluoroboric acidHCID 143652502,3-Dichloro-4,5-difluoroanilineHCID 23668193Sodium Nitrite

Product 1

HCID 143652512,3-Dichloro-4,5-difluorobenzenediazonium tetrafluoroborate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a suspension of 2,3-dichloro-4,5-difluoroaniline (0.88 g) in 42% fluoroboric acid (10 ml) with stirring vigorously was added sodium nitrite (0.43 g) in water (1 ml) at -15° to 0° C. for 14 minutes. After stirred for 3 hours at the same temperature, the resulting precipitate was collected by filtration, washed with 42% fluoroboric acid and then with ether to give the title compound (0.66 g) as white powdery crystals, mp 211° C.-(decompd.).

Workup

  1. stirringAfter stirred for 3 hours at the same temperature
  2. filtrationthe resulting precipitate was collected by filtration
  3. washwashed with 42% fluoroboric acid

Sources & evidence

ORD record
ord-c00c957a64f143c5a1157111cdfb6301
Source dataset
uspto-grants-1988_12
Patent number
US04791225

Reaction notes

Loading…