Methanol → HCID 178462740, compound
Reaction equation
[CH:1]([N:3]1[CH:7]=[CH:6][N:5]=[CH:4]1)=[CH2:2].[CH2:8]([Br:20])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].CO>C(OCC)C>[Br-:20].[CH:1]([N+:3]1[CH:7]=[CH:6][N:5]([CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH3:8])[CH:4]=1)=[CH2:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
(From Yuan & Antonietti, DOI: 10.1021/ma102858b.) A solution/suspension comprising 0.1 mol of 1-vinylimidazole, 0.1 mol of n-dodecyl bromide and 30 mL of methanol were loaded into a 100 mL reactor. The mixture was stirred at 60° C. for 15 h. After cooling the reaction mixture was added dropwise into 1 L of diethyl ether. The white precipitate was filtered off and dried at room temperature to yield a powder.
Workup
- customwere loaded into a 100 mL reactor
- temperatureAfter cooling the reaction mixture
- filtrationThe white precipitate was filtered off
- customdried at room temperature
- customto yield a powder
Sources & evidence
- ORD record
- ord-1f36f05c996147e8a4ec03e260357161
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08920682B2
Reaction notes
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