Ethylene Glycol → HCID 66918225, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([B:9]([OH:11])[OH:10])[CH:6]=[CH:7][CH:8]=1)#[N:2].[CH2:12](O)[CH2:13][OH:14].CCCCCC>C1COCC1>[B:9]([O:11][CH2:12][CH2:13][OH:14])([OH:10])[C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([C:1]#[N:2])[CH:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Cyanophenyl boronic acid (1 g, 6.8 mmol) was dissolved in dry THF (10 mL) under nitrogen. Ethylene glycol (379 μL, 422 mg, 6.8 mmol) was added and the reaction was heated to reflux for 4 hours then cooled to room temperature. THF was removed by rotary evaporator to give a white solid. Cold hexane was added and the product was collected by filtration giving a white solid (1.18 g, quant. yield). 1H-NMR (300.058 MHz, DMSO-d6) δ ppm 7.92-8.01 (3H, m), 7.50-7.64 (1H, m), 4.35 (4H, s)
Workup
- temperaturethe reaction was heated
- temperatureto reflux for 4 hours
- customTHF was removed by rotary evaporator
- customto give a white solid
- filtrationthe product was collected by filtration
Sources & evidence
- ORD record
- ord-dc10b87dc11b460da9ed14f67b027ea8
- Source dataset
- uspto-grants-2008_06
- Patent number
- US07390806B2
Reaction notes
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