HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852391Generated: October 31, 2026
Ethanesulfonyl chloride → HCID 67073865, compound
https://huagongshe.com/reaction/1852391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | HCID 67074413 | HCID 67074413 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67073865 | HCID 67073865 | 118% |
Reaction Steps
1.18 g 3-(3-amino-2-methylphenoxy)-5-fluoro-N-(2-fluoro-4-iodophenyl)-2-nitroaniline (2.3 mmol, 1 eq.) were dissolved in 9.6 mL pyridine, cooled to 0° C., treated with 292 μL ethyl sulfonyl chloride (3.1 mmol, 1.2 eq.) and stirred at 0° C. for 3 hours. The reaction mixture was diluted with toluene and concentrated in vacuo. The residue was partitioned between water and ethyl acetate. The aqueous layer was reextracted with ethyl acetate. The combined organic layers were dried, filtered and concentrated in vacuo to yield 1.6 g of the crude product, which was taken up in toluene and again concentrated in vacuo. The crude product was used in the subsequent transformations without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962606B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-c368f4071e464d6098f69d58be5101cc |
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| Source note | uspto-grants-2015_02 |
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