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HRID 1074085作成日:2026年10月25日

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

https://huagongshe.com/reaction/1074085

反応式

関与物質

役割名称HCID仕込み量
反応物Triethyloxonium tetrafluoroborateHCID 2723982—
反応物t-Butyl 4-dimethylamino-2-oxo-3-butenoateHCID 53856676—
反応物N-(3-ethoxy-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743577—
溶媒DichloromethaneHCID 6344—
生成物N-(3-ethoxy-3-t-butyloxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743597—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04971979
出典データセットuspto-grants-1990_11
ORD IDord-7413cd2e4b7f42ab8f154606708c15aa
出典メモuspto-grants-1990_11