HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675320Generated: October 30, 2026
Nitrobenzene → 3-Nitrobenzenesulfonyl chloride
https://huagongshe.com/reaction/1675320
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | 3-Nitrobenzenesulfonyl chloride | HCID 8476 | — |
Reaction Steps
Chlorosulfonic acid (4.16 mmol, 0.475 grams) was taken in 1 L three neck round bottom flask equipped with a guard tube and liquid addition funnel. Chlorosulfonic acid was cooled in ice bath to 5-10° C. and nitrobenzene (0.83 mmol, 0.102 grams) was added to the acid slowly, at such a rate that the temperature maintained below 10° C. Reaction mixture was then brought to 25° C. and then slowly heated in an oil bath to 80-85° C. The above reaction mixture was stirred further at 80-85° C. for a period of 3 hours. After completion of the reaction, the reaction mixture was cooled to 10° C. and poured on to the ice-water mixture under stirring, while maintaining the temperature below 10° C. The resulting slurry was then filtered on buchner funnel. The solid cake was dried on phosphorous pentoxide in a desiccator to obtain the title compound as off white solid. Yield: 0.144 grams.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003670B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-af1058c5f35946a8b72d4c3b2c54713d |
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| Source note | uspto-grants-2011_08 |
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