Ethyl vinyl ether → 3-(1-Ethoxyethoxy)-3-methyl-butane-2-one
Reaction equation
[CH3:1][C:2]([OH:7])([CH3:6])[C:3](=[O:5])[CH3:4].[CH2:8]([O:10][CH:11]=[CH2:12])[CH3:9]>C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.C(Cl)Cl>[CH2:8]([O:10][CH:11]([O:7][C:2]([CH3:6])([CH3:1])[C:3](=[O:5])[CH3:4])[CH3:12])[CH3:9]Participants
Procedure
In a 200 ml three-necked flask equipped with a mechanical stirrer, dropping funnel, reflux condenser, and a nitogen-inlet tube, 15 gm (147 mmol) of 3-methyl-3-hydroxy-2-butanone, 500 mg (2.0 mmol) of pyridinium p-toluenesulfonate and 100 ml of anhydrous methylenechloride were mixed with stirring under nitrogen stream, and 11.7 gm (162 mmol) of ethylvinylether was added dropwise at room temperature for 3 hours while stirring. After the reaction, the reaction mixture was washed with 5% aqueous sodium hydrogencarbonate, and then the mixture was extracted with chloroform. The extract was dried over anhydrous sodium sulfate and the solvent was removed by evaporation to give a crude product. Distillation of the crude product afforded 17.09 gm of 3-(1-ethoxyethoxy)-3-methyl-butane-2-one (b.p. 38-40/1 mmHg, yield: 66%).
Workup
- customIn a 200 ml three-necked flask equipped with a mechanical stirrer
- temperaturereflux condenser, and a nitogen-inlet tube
- additionwas added dropwise at room temperature for 3 hours
- customAfter the reaction
- washthe reaction mixture was washed with 5% aqueous sodium hydrogencarbonate
- extractionthe mixture was extracted with chloroform
- dry with materialThe extract was dried over anhydrous sodium sulfate
- customthe solvent was removed by evaporation
- customto give a crude product
- distillationDistillation of the crude product
Sources & evidence
- ORD record
- ord-d4d54218eb2b42959e46421c03f169bd
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05146002
Reaction notes
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