HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667587Generated: October 29, 2026
AcOH AcOAc → N-[3-Cyano-4-(ethanesulfonyl)phenyl]acetamide
https://huagongshe.com/reaction/1667587
Participants
| Role | Name | HCID | Charge |
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| Reactant | AcOH AcOAc | HCID 21895370 | — |
| Reactant | 2-(Ethanesulfonyl)-5-nitrobenzonitrile | HCID 57448182 | — |
| Catalyst | Iron | HCID 23925 | — |
| Product | N-[3-Cyano-4-(ethanesulfonyl)phenyl]acetamide | HCID 57448183 | 83% |
Reaction Steps
To 5B (3.60 g, 15.0 mmol) in 1:1 acetic acid/acetic anhydride (150 mL), Fe (4.20 g, 75.2 mmol) was added. The reaction mixture was heated to 100° C. for 2 h then poured into ice. After the ice melted, the product was extracted with ethyl acetate, and the organic layer was washed with saturated aqueous NaHCO3 and brine. The organic layer was dried (Na2SO4), filtered and concentrated to provide 5C (3.14 g, 83%). LC-MS: 241.18 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044242B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-0cbc4430504741bbaca3cef9e5e9c921 |
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| Source note | uspto-grants-2011_10 |
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