N,N'-Dimethylethylenediamine → n-(2,4-Difluorophenyl)-n,n'-dimethylethylene-1,2-diamine
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[F:9].[CH3:10][NH:11][CH2:12][CH2:13][NH:14][CH3:15].O(C(C)(C)C)[Na]>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd]>[F:9][C:3]1[CH:4]=[C:5]([F:8])[CH:6]=[CH:7][C:2]=1[N:11]([CH3:10])[CH2:12][CH2:13][NH:14][CH3:15]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Combine 1-bromo-2,4-difluorobenzene (1.00 g, 5.18 mmol), N,N′-dimethyl-ethylenediamine (2.74 g, 31.1 mmol), NaO-t-Bu (0.70 g, 7.2 mmol), Pd(dba)2 (0.060 g, 0.10 mmol) and (±)-BINAP (0.19 g, 0.31 mmol) in toluene (10 ml). Heat at 110° for 18 h, allow to cool, and extract with 1N HCl. Basify the aqueous solution with NaOH and extract with CH2Cl2. Dry, concentrate, and purify by PLC to give N-(2,4-difluoro-phenyl)-N,N′-dimethylethylenediamine.
Workup
- temperatureHeat at 110° for 18 h
- temperatureto cool
- extractionextract with 1N HCl
- extractionextract with CH2Cl2
- customDry
- concentrationconcentrate
- custompurify by PLC
Sources & evidence
- ORD record
- ord-bbd07389113042f8ba7bcb23146a38a4
- Source dataset
- uspto-grants-2003_10
- Patent number
- US06630475B2
Reaction notes
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