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HRID 224421作成日:2026年10月25日

Toluene → (S)-(-)-2-((3-Bromo-2,6-dimethoxybenzamido)methyl)-1-ethylpyrrolidine hydrochloride

https://huagongshe.com/reaction/224421

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Thionyl ChlorideHCID 24386—
反応物2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
反応物3-Bromo-2,6-dimethoxybenzoic acidHCID 2774744—
溶媒Diethyl EtherHCID 3283—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物(S)-(-)-2-((3-Bromo-2,6-dimethoxybenzamido)methyl)-1-ethylpyrrolidine hydrochlorideHCID 15565708—

反応手順

30 ml of thionyl chloride is added to 17.6 g (0.067 mol) of 3-bromo-2,6-dimethoxybenzoic acid. The mixture is heated on a steam bath for 30 minutes. To the solution is added 50 ml of toluene. The solvent and excess thionyl chloride is evaporated at reduced pressure. The residue is dissolved in 50 ml of dry methyl ethyl ketone. The solution is added dropwise while stirring to 9.23 g (0.072 mol) of 2-(aminomethyl)-1-ethylpyrrolidine in 50 ml of methyl ethyl ketone. After stirring for 30 minutes at room temperature 150 ml of ethyl ether is added. The obtained precipitate is filtered off, washed with ether and recrystallized twice from ethanol-isopropyl ether. Yield: 21.0 g, m.p. 182°-84° C. (first recrystallization). m.p. 184°-85° C. (second recrystallization).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04232037
出典データセットuspto-grants-1980_11
ORD IDord-26f7e6a3387244f3ba271f5c15ea707f
出典メモuspto-grants-1980_11