HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292251Generated: October 30, 2026
Sulfuric Acid → 2-Bromo-1-fluoro-4-nitrobenzene
https://huagongshe.com/reaction/2292251
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-1-fluoro-4-nitrobenzene | HCID 69699 | — |
Reaction Steps
28.2 g of p-fluoro-nitrobenzene were added to 20° C. to 10.4 ml of bromine and then 20 ml of water followed by 180 ml of concentrated sulfuric acid were added thereto at 0° C. 34 g of silver sulfate were added to the mixture and the temperature was allowed to rise to 20°-25° C. and the mixture was stirred for 16 hours and was poured into water. The mixture was filtered and the filter was washed with water and methylene chloride. The filtrate was extracted with methylene chloride and the organic phase was washed with water, dried over magnesium sulfate, filtered and evaporated to dryness under reduced pressure. The residue was dissolved in isopropyl ether and crystallized therefrom. The mixture was filtered and the product was washed to obtain 8.2 g of 3-bromo-4-fluoro-nitrobenzene melting at 59° C. Using the procedure of Example 1, the latter was reacted to obtain 0-(4-nitro-2-bromo-phenyl)-hydroxylamine melting at 122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801717 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-db608ffa91ec4957b71666d6403cbc06 |
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| Source note | uspto-grants-1989_01 |
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