HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477300Generated: October 25, 2026
Triethyloxonium tetrafluoroborate → N-(3-ethoxy-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate
https://huagongshe.com/reaction/477300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | Ethyl 4-(dimethylamino)-2-oxo-but-3-enoate | HCID 2777802 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-ethoxy-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate | HCID 86743577 | — |
Reaction Steps
Ethyl 4-dimethylamino-2-oxo-3-butenoate (675 g) is added in the course of 3 hours, while the temperature is maintained at approximately 10° C., to a solution, cooled to 10° C. and through which a stream of argon is passed, of triethyloxonium tetrafluoroborate (862 g) in methylene chloride. The reaction medium is then stirred for 5 hours at a temperature in the region of 20° C. The solution of N-(3-ethoxy-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate thereby obtained is stored under an argon atmosphere, and is used immediately in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886835 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-e38d764ecb1948b397dd6064dd1d53e2 |
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| Source note | uspto-grants-1989_12 |
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