HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720763Generated: October 29, 2026
Sulfuric Acid → 7-Bromodibenzothiophene-3-ol
https://huagongshe.com/reaction/720763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 7-Bromodibenzothiophene-3-yl-amine | HCID 21895087 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Bromodibenzothiophene-3-ol | HCID 21894920 | — |
Reaction Steps
A flask equipped with a stirrer and a thermometer was charged with 209.3 g of concentrated sulfuric acid and 8.93 g of NaNO2 in a nitrogen atmosphere, and cooled to 2° C. Then 24.0 g of the intermediate 7-bromodibenzothiophene-3-yl-amine prepared in Example 1-3 was added, and stirred at 2 to 4° C. for 3 hours. The resulting mixture together with 99.8 g of water was poured into 348.7 g of 65 wt % sulfuric acid preheated to 80° C., stirred at 80 to 85° C. for 5 hours, and cooled to room temperature. The reactant was filtered, extracted six times with 300 ml of ethyl acetate, and vacuum concentrated. The concentrate was purified by silica gel chromatography using chloroform as an eluting solvent to obtain 7.11 g of objective 7-bromodibenzothiophene-3-ol. The 1H-NMR spectrum data and the results of elemental analysis of the product are shown below:
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-7b245a96f12748eca039d7bf64d0b666 |
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| Source note | uspto-grants-2006_11 |
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