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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224421Generated: October 25, 2026

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

https://huagongshe.com/reaction/224421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
Reactant3-Bromo-2,6-dimethoxybenzoic acidHCID 2774744—
SolventDiethyl EtherHCID 3283—
SolventMethyl Ethyl KetoneHCID 6569—
Product(S)-(-)-2-((3-Bromo-2,6-dimethoxybenzamido)methyl)-1-ethylpyrrolidine hydrochlorideHCID 15565708—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232037
Source datasetuspto-grants-1980_11
ORD IDord-26f7e6a3387244f3ba271f5c15ea707f
Source noteuspto-grants-1980_11