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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477364Generated: October 25, 2026

Triethyloxonium tetrafluoroborate → N-(3-ethoxy-3-t-butyloxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate

https://huagongshe.com/reaction/477364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactantt-Butyl 4-dimethylamino-2-oxo-3-butenoateHCID 53856676—
ReactantN-(3-ethoxy-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743577—
SolventDichloromethaneHCID 6344—
ProductN-(3-ethoxy-3-t-butyloxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743597—

Reaction Steps

The procedure is as in Example 2 for the preparation of N-(3-ethoxy-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate, starting with t-butyl 4-dimethylamino-2-oxo-3-butenoate (3.3 g) and triethyloxonium tetrafluoroborate (3.62 g) in dichloromethane (20 cc). The solution of N-(3-ethoxy-3-t-butyloxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate in methylene chloride thereby obtained is stored under an argon atmosphere and used immediately in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886835
Source datasetuspto-grants-1989_12
ORD IDord-421d381728ea43cf9447d26808ddd725
Source noteuspto-grants-1989_12