HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720761Generated: October 29, 2026
Nitric Acid → 3-Bromo-7-nitrodibenzothiophene-5-oxide
https://huagongshe.com/reaction/720761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Bromodibenzothiophene-5-oxide | HCID 21895132 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-7-nitrodibenzothiophene-5-oxide | HCID 21895096 | — |
Reaction Steps
A flask equipped with a stirrer and a thermometer was charged with 69.8 g of glacial acetic acid and 27.9 g of 3-bromodibenzothiophene-5-oxide prepared in Example 1-1 in a nitrogen atmosphere, and cooled to 10° C. 239.8 g of concentrated sulfuric acid was added dropwise, and the resulting mixture was cooled to −2° C. Then 72.0 g of 70 wt % nitric acid was added dropwise at −2 to 8° C., and the resulting mixture was stirred at or below 5° C. for 2 hours. The reaction mass was poured into 1200 g of ice water to terminate the reaction, and stirred further. The reactant was filtered, washed with water, and dried. The resulting dry cake was washed with ethanol to obtain 31.9 g of 3-bromo-7-nitrodibenzothiophene-5-oxide. The product was subjected to elemental analysis, the results of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135579B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-0bc663e56fdb4653a3ac9366847d8215 |
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| Source note | uspto-grants-2006_11 |
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