HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110832Generated: November 2, 2026
Borane;tetrahydrofuran → 4-Aminomethyl-1-(1-naphthylsulfonyl)piperidine
https://huagongshe.com/reaction/2110832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 1-(Naphthylsulfonyl)piperidine-4-carboxamide | HCID 23993292 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Aminomethyl-1-(1-naphthylsulfonyl)piperidine | HCID 68862030 | 90% |
Reaction Steps
To a solution of 4-aminocarbonyl-1-(1-naphthylsulfonyl)piperidine (10.6 g, 33.3 mmol) in tetrahydrofuran (200 mL) stirring under argon at room temperature, was added borane-tetrahydrofuran complex (1.5 M in tetrahydrofuran, 67 mL, 100 mmol). The resulting solution was heated to 80° C. for 6 h before the solvent was evaporated under vacuum. The residue was dissolved in 1.0 M aqueous hydrochloric acid (100 mL), and this was washed with diethyl ether (100 mL twice). The aqueous layer was basified to pH 10 with 50% aqueous sodium hydroxide and extracted with dichloromethane (50 mL three times). The combined dichloromethane extracts were dried (anhydrous sodium sulfate) and evaporated under vacuum to obtain 4-aminomethyl-1-(1-naphthylsulfonyl)piperidine (9.1 g, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517991B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-96211a1ab580490d902bc8dbc4f521a4 |
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| Source note | uspto-grants-2009_04 |
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