HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10352Generated: October 26, 2026
Hydrochloric Acid → 1-(1-Benzyl-3-methoxymethylpyrrolidin-3-yl)methylamine
https://huagongshe.com/reaction/10352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-(1-Benzyl-3-methoxymethylpyrrolidin-3-ylmethyl)isoindole-1,3-dione | HCID 57832637 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1-Benzyl-3-methoxymethylpyrrolidin-3-yl)methylamine | HCID 21978971 | 89.5% |
Reaction Steps
Hydrazine hydrate (85% solution in water, 0.372 g, 6.32 mmol) is added to a solution of 2-(1-benzyl-3-methoxymethylpyrrolidin-3-ylmethyl)isoindole-1,3-dione (Example A20, 1.581 g, 4.34 mmol) in ethanol (50 mL). The resulting mixture is refluxed for 4.5 hours, cooled and acidified with concentrated hydrochloric acid. The precipitate is removed by filtration and the filtrate is concentrated in vacuo. The residue is dissolved in ethanol/water (2:1) and the insoluble material is removed by filtration. The filtrate is basified to pH 10 with 1N sodium hydroxide solution and extracted with dichloromethane. The combined organic extracts are dried over Na2SO4, filtered and concentrated under vacuum to afford the title compound (0.910 g). 1H NMR (200 MHz, CDCl3): δ 7.41–7.15 (m, 5H), 3.57 (s, 2H), 3.33 (s, 3H), 3.30 (s, 2H), 2.71 (s, 2H), 2.64–2.51 (m, 2H), 2.42–2.24 (m, 2H), 1.68–1.52 (m, 2H), 1.38–1.10 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094780B1 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-bb473ca2021b44e6ad238522ab891e1c |
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| Source note | uspto-grants-2006_08 |
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