Acetonitrile → HCID 53671371, compound

HRID 716072Notes

Reaction equation

HRID 716072 reaction equation
[C:1]([O-])([O-])=O.[K+].[K+].[Br:7][C:8]1[CH:9]=[C:10]([CH:12]=[CH:13][CH:14]=1)[NH2:11].[CH2:15](Br)[CH:16]=[CH2:17].[C:19](#N)[CH3:20]>>[Br:7][C:8]1[CH:9]=[C:10]([CH:12]=[CH:13][CH:14]=1)[N:11]([CH2:1][CH:19]=[CH2:20])[CH2:15][CH:16]=[CH2:17]

Participants

5

Reactant 4

HCID 6342AcetonitrileHCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 115623-Bromoaniline

Product 1

HCID 53671371HCID 53671371, compoundYield 85%

Conditions

Temperature
80 °C

Procedure

K2CO3 (22.0 g, 159 mmol) was suspended in acetonitrile, the suspension was added with 3-bromoaniline (8.71 mL, 80.0 mmol) and allyl bromide (23.7 mL, 280 mmol), and the mixture was stirred at 80° C. for 14 hours. The reaction mixture was cooled to room temperature, then filtered through Celite, and sufficiently washed with ethyl acetate. The solvent was removed, and then the residue was purified by column chromatography (silica gel, ethyl acetate/hexane (1/40)) to obtain 3-bromo-N,N-diallylaniline (17.1 g, 67.9 mmol, yield 85%).

Workup

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationfiltered through Celite
  3. washsufficiently washed with ethyl acetate
  4. customThe solvent was removed
  5. customthe residue was purified by column chromatography (silica gel, ethyl acetate/hexane (1/40))

Sources & evidence

ORD record
ord-86da58d15a0a4aec962c87b02333bdb1
Source dataset
uspto-grants-2015_11
Patent number
US09187499B2

Reaction notes

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