HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891713Generated: October 28, 2026
Sodium Azide → 4-Azido-1-(p-nitrobenzyloxycarbonyl)piperidine
https://huagongshe.com/reaction/891713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-Methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)piperidine | HCID 22242766 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Azido-1-(p-nitrobenzyloxycarbonyl)piperidine | HCID 22242714 | 100% |
Reaction Steps
To a solution of 4-methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)piperidine (3.31 g, 9.24 mmol) (obtained as described in Reference Example 51(2)) in dimethylformamide (100 ml) was added sodium azide (660 mg, 10.2 mmol), and the mixture was stirred in an oil bath (100° C.) for 3 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (3:1→1:1) as the eluant to afford 4-azido-1-(p-nitrobenzyloxycarbonyl)piperidine (2.81 g, yield 100%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-ee2f0db8f5394a69917cf025070d9a0c |
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| Source note | uspto-grants-2006_02 |
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