Sodium Carbonate → [1,1':2',1''-Terphenyl]-2-amine

HRID 1797387Notes

Reaction equation

HRID 1797387 reaction equation
Br[C:2]1[CH:8]=[CH:7][CH:6]=[C:5](Br)[C:3]=1[NH2:4].[C:10]1(B(O)O)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1.CCO.O.CCOCC.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:2]1([C:11]2[C:10]([C:2]3[CH:8]=[CH:7][CH:6]=[CH:5][CH:3]=3)=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:3]([NH2:4])=[CH:5][CH:6]=[CH:7][CH:8]=1

Participants

9

Reactant 3

HCID 10340Sodium Carbonate2×HCID 66827Phenylboronic AcidHCID 690982,6-Dibromoaniline

Product 1

HCID 12595497[1,1':2',1''-Terphenyl]-2-amineYield 90%

Reagents, catalysts & solvents 5

HCID 178418397HCID 178418397, compoundCatalystHCID 702EthanolSolventHCID 962WaterSolventHCID 1140TolueneSolventHCID 3283Diethyl EtherSolvent

Procedure

2,6-Dibromoaniline (6.02 g, 24 mmol) and Pd(PPh3)4 (3.88 g, 3.00 mmol) were dissolved in toluene (240 ml). Phenyl boronic acid (8.80 g, 72 mmol) in EtOH (50 ml) was added. Na2CO3 (13 g, 144 mmol) in H2O (70 ml) was added. The reaction mixture was reflux for 24 hrs. The organic layer was thin separated and the amine precipitated as hydrochloride salt by addition of 20 ml of HCl. The precipitate was isolated. The salt was suspended in ether, and 2 M Na2CO3 was added. The organic layer was dried over Na2SO4 and the solvent was evaporated. The yield was 90%. 1H NMR (CDCl3): δ 7.44 (t, 4H, Harom), 7.39 (t, 4H, Harom), 7.29 (d, 2H, Harom), 7.07 (d, 2H, Harom), 6.82 (t, 1H, Harom), 3.77 (s, 2H, NH2).

Workup

  1. temperatureThe reaction mixture was reflux for 24 hrs
  2. customThe organic layer was thin separated
  3. customthe amine precipitated as hydrochloride salt by addition of 20 ml of HCl
  4. customThe precipitate was isolated
  5. dry with materialThe organic layer was dried over Na2SO4
  6. customthe solvent was evaporated

Sources & evidence

ORD record
ord-1fcad542f0344c99b2dab2bb67a279b4
Source dataset
uspto-grants-2006_04
Patent number
US07034157B2

Reaction notes

Loading…