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HRID 67180作成日:2026年10月26日

Epichlorohydrin → 2-Ethoxy-1-methylquinolinium fluoroborate

https://huagongshe.com/reaction/67180

反応式

関与物質

役割名称HCID仕込み量
反応物EpichlorohydrinHCID 7835—
反応物Boron trifluoride etherateHCID 8000—
反応物1-Methyl-2-quinoloneHCID 11820—
反応物Triethyloxonium tetrafluoroborateHCID 2723982—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物Triethyloxonium tetrafluoroborateHCID 2723982—
生成物2-Ethoxy-1-methylquinolinium fluoroborateHCID 1305945483.5%

反応手順

Triethyloxonium fluoroborate is prepared from 3.70 g (0.040 mole) of epichlorohydrin in 14 ml of ether and 7.58 g (0.054 mole) of boron trifluoride etherate in 6 ml of ether. The resulting solid triethyloxonium fluoroborate is dissolved in 20 ml of dry methylene chloride and treated under nitrogen with 6.47 g (0.040 mole) of N-methyl-2-quinolone in 15 ml of methylene chloride. The reaction mixture is stirred under nitrogen at room temperature overnight. The solid is filtered to give 9.2 g (83.5%) of 2-ethoxy-1-methylquinolinium fluoroborate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04345083
出典データセットuspto-grants-1982_08
ORD IDord-cbe2d123b31448a7962b73e59b07b8b2
出典メモuspto-grants-1982_08