HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870813Generated: October 29, 2026
2-Nitrobenzenesulfonyl chloride → N-(Benzyloxy)-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/870813
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(Benzyloxy)-2-nitrobenzenesulfonamide | HCID 9839578 | 69.6% |
Reaction Steps
A solution of 2-nitrobenzene-1-sulfonyl chloride (500 g, 2.26 mol) in pyridine (1500 mL) was added dropwise to a solution of O-benzylhydroxylamine hydrochloride (400 g, 2.51 mol) in pyridine (1500 mL) at 0° C. The reaction mixture was then stirred at 20° C. overnight. The mixture was concentrated in vacuum, diluted with DCM and washed with HCl (10%) three times. The combined organic layer was concentrated in vacuum and re-crystallized with DCM to afford N-(benzyloxy)-2-nitrobenzenesulfonamide (485 g, 62.6%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969570B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-558b40aed3a24b5c98686a41154af3a5 |
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| Source note | uspto-grants-2015_03 |
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