HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526723Generated: October 31, 2026
Water → N-benzyl-N-(4-bromo-3-oxobutyl)-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/526723
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-benzyl-2-nitro-N-(3-oxobutyl)benzenesulfonamide | HCID 71152136 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzyl-N-(4-bromo-3-oxobutyl)-2-nitrobenzenesulfonamide | HCID 71502814 | 53.1% |
Reaction Steps
To a solution of N-benzyl-2-nitro-N-(3-oxobutyl)benzenesulfonamide (compound F, 30 g, 83 mmol) in methanol (300 ml) was added bromine (4.69 ml, 91 mmol) in one portion at 20-25° C. Stirred for 20 hours (no bromine colour), water (20 ml) added, heated to reflux for 30 min, diluted with MeOH (100 ml). The solution was cooled to 30° C. with stirring, seeded with compound G, stirred at 25-30° C. for 5 min (crystallisation occurred), cooled to 15° C., aged for 1 hour. Crystals collected, washed with 2×15 ml of MeOH (20-25° C.), dried on air to give N-benzyl-N-(4-bromo-3-oxobutyl)-2-nitrobenzenesulfonamide (19.4 g, 44.0 mmol, 53.1% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346751B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-370cf6944fec4aaea716719aca1f5a39 |
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| Source note | uspto-grants-2016_05 |
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