HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754115Generated: November 1, 2026
4-Nitrobenzenesulfonyl chloride → HCID 27301538, compound
https://huagongshe.com/reaction/1754115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | 2-(Trifluoromethoxy)aniline | HCID 73754 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 27301538 | HCID 27301538 | 76.6% |
Reaction Steps
To a pre-cooled solution of 2-(trifluoromethoxy)aniline (1.8 g, 10.16 mmol) in pyridine (20 ml) was added 4-nitrobenzene-1-sulfonyl chloride (2.252 g, 10.16 mmol) in 5-10 mL of pyridine at 0° C. slowly. The reaction mixture was stirred and heated to 85° C. for 3 h, then cooled down to 45° C. and stirred at the same temperature over weekend. The solvent was removed under reduced pressure. The residue was diluted with methylene chloride and washed with 1N HCl (×2), water (×2), and brine. The organic layer was separated, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to give 2.82 g of title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169209B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-1d27b79954944e76b47e122f20afdc49 |
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| Source note | uspto-grants-2015_10 |
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