HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841920Generated: October 29, 2026
4-Nitrobenzenesulfonyl chloride → N-((4-Nitrophenyl)sulfonyl)-1-(tert-butyloxycarbonyl)piperazine
https://huagongshe.com/reaction/1841920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-((4-Nitrophenyl)sulfonyl)-1-(tert-butyloxycarbonyl)piperazine | HCID 10595407 | 97.8% |
Reaction Steps
Diisopropylethylamine (7.8 ml, 45 mmol) was added in one portion to a stirred solution of piperazine-1-carboxylic acid tert-butyl ester (7.6 g, 41 mmol) in DCM (100 ml) at room temperature. To this mixture was added 4-nitrophenyl sulfonyl chloride (10.0 g, 45 mmol) in one portion and the mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After this time the mixture was diluted with DCM (50 ml) and washed with water (100 ml), saturated NaHCO3 (100 ml) and HCl (100 ml, 2M). The organic layer was separated, dried (MgSO4), filtered and concentrated under vacuum to give the title compound (14.9 g, 89% yield) as a white solid. δH (500 MHz, DMSO) 8.45 (2H, d), 7.97 (2H, d), 3.34 (4H, obscured), 2.96-2.92 (4H, m), 1.33 (9H, s). Tr=1.91 min m/z (ES+) ([(M−100)+H]+) 272.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946197B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-242135966e4c4d0d9825c7fd476cb49c |
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| Source note | uspto-grants-2015_02 |
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