HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10526Generated: October 25, 2026
tert-Butyl 4-oxopiperidine-1-carboxylate → 1-Boc-4-(aminomethyl)piperidine
https://huagongshe.com/reaction/10526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | 93.9% |
Reaction Steps
A solution of methylamine hydrochloride (1.01 g, Wako Pure Chemical Industries) and 1-(tert-butoxycarbonyl)-4-oxopiperidine (1.99 g, Aldrich) in methanol (13 ml) was stirred in the presence of platinum oxide (69 mg, Wako Pure Chemical Industries) at room temperature for 3 hours under hydrogen atmosphere of ordinary pressure. The hydrogen was purged with a nitrogen gas, and the platinum catalyst was removed by filtration. Then, the reaction mixture was adjusted to pH of from 10 to 11 with 1 N aqueous sodium hydroxide. The reaction mixture was added with water (10 ml), and the product was extracted three times with ethyl acetate (15 ml for each time). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:methanol=20:1) to obtain the title compound (2.01 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094789B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-d468fd2f35634bbfb59c0f3c2c17ef5c |
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| Source note | uspto-grants-2006_08 |
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