HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176563Generated: October 30, 2026
Methylamine → 1-[(3R)-1-Benzylpyrrolidin-3-yl]methanamine
https://huagongshe.com/reaction/1176563
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | (S)-1-Benzyl-3-[(P-tolylsulfonyl)oxy]pyrrolidine | HCID 10382042 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[(3R)-1-Benzylpyrrolidin-3-yl]methanamine | HCID 1519423 | — |
Reaction Steps
An autoclave is initially charged with 6.20 ml of methylamine solution in ethanol and a solution of 2.000 g of (S)-1-benzylpyrrolidin-3-yl toluene-4-sulphonate in 2 ml of ethanol. The reaction solution is subsequently heated to 140° C. over 15 hours. The reaction solution is cooled to room temperature and concentrated to dryness, and the residue is taken up in 10 ml of water. The aqueous solution is extracted with dichloromethane (2×10 ml). The aqueous phase is then admixed with 1 g of potassium carbonate and the suspension is stirred at room temperature over 5 minutes. The solid is filtered off and the filtrate is extracted with dichloromethane (2×10 ml). The combined organic phases are dried over sodium sulphate and concentrated by evaporation. The residue is purified by means of flash chromatography (SiO2 60F). The title compound is obtained as a yellow oil. Rf=0.14 (200:20:1 dichloromethane-methanol-25% conc. ammonia).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842688B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-031e71327128424cb2bf0016f3462b95 |
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| Source note | uspto-grants-2010_11 |
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