HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322486Generated: October 29, 2026
Trimethylamine → 1-(Naphthalene-1-sulfonyl)-pyrrolidin-3-ylamine
https://huagongshe.com/reaction/322486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-Naphthalenesulfonyl chloride | HCID 66560 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl pyrrolidine-3-carboxylate | HCID 22394392 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 1-(Naphthalene-1-sulfonyl)-pyrrolidin-3-ylamine | HCID 57241802 | 23% |
Reaction Steps
To a solution of 1-naphthalenesulfonyl chloride (1.0 g, 5.4 mmol) in 50 ml of CH2Cl2 with 2 ml of trimethylamine was added 3-t-butoxycarbonylpyrrolidine (1.5 g, 6.5 mmol) in a portion and the resulting solution was stirred at reflux for 48 h. Reaction mixture was concentrated in vacuo, yielding oily mixture which was partioned between 100 ml of EtOAc and NaHCO3 sat'd aqueous solution. Organic layer was separated, dried over Na2SO4 and concentrated in vacuo to provide an oil, which was redissolved in 20 ml of CH2Cl2. Toward this solution was added 1 ml of trifluoroacetic acid and the resulting solution was stirred for 2 h at 25° C. Reaction mixture was concentrated in vacuo, providing a brown oil, which was dissolved in EtOAc and washed with aqueous NaOH. organic layer was concentrated in vacuo to yield an oil which was subjected to column chromatography (30% MeOH/CHCl3) to provide 0.17 g (23%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211241B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-babfea74bc6a43e3af053c0b6d2b5277 |
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| Source note | uspto-grants-2001_04 |
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