HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885770Generated: October 26, 2026
Ethyl vinyl ether → 3-(1-Ethoxyethoxy)-3-methyl-butane-2-one
https://huagongshe.com/reaction/1885770
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | 3-Hydroxy-3-methyl-2-butanone | HCID 8261 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(1-Ethoxyethoxy)-3-methyl-butane-2-one | HCID 19777564 | 66.7% |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05146002 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-d4d54218eb2b42959e46421c03f169bd |
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| Source note | uspto-grants-1992_09 |
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