1,3-Dimethoxybenzene → HCID 14341015, compound
Reaction equation
[P:1]([Br:4])(Br)[Br:2].[CH3:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[CH:8]=1>N1C=CC=CC=1>[Br:2][P:1]([Br:4])[C:10]1[CH:11]=[CH:12][C:7]([O:6][CH3:5])=[CH:8][C:9]=1[O:13][CH3:14]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of PBr3 (2.5 g, 9.2 mm) in 15 mL of pyridine was treated with 1,3-dimethoxybenzene (2.5 g, 18.1 mm) over a period of 5 min. The resulting mixture was then refluxed for 4 h. to give the crude 1-dibromophosphino-2,4dimethoxybenzene (31P NMR: δ159.2 ppm). This compound was used directly for the next step without further purification. Next, polymer-supported secondary amines from Example 1 (10.0 g, 1.1 mmol/g, 11.0 mmol) was slowly added into the mixture above while stirring at room temperature for a period of 10 min. The resulting suspension was stirred at room temperature overnight before the solution was filtered off. The resin was washed with THF (50 mL), hexane (3×50 mL), CH2Cl2 (4×50 mL), and hexane (2×50 mL). The resulting resin was dried in vacuum overnight to yield the polymer-supported 2-P(Br)-1,5-(MeO)2-C6H3. 31P NMR (122 MHz, CDCl3): δ153.8 ppm.
Workup
- temperatureThe resulting mixture was then refluxed for 4 h.
Sources & evidence
- ORD record
- ord-8090a7735b684860805b30f5ac5aa965
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716984B2
Reaction notes
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