HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432966Generated: October 31, 2026
Ethyl Acetate → N-(3-amino-4-fluorophenyl)-1-chloromethanesulfonamide
https://huagongshe.com/reaction/432966
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide | HCID 18760842 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(3-amino-4-fluorophenyl)-1-chloromethanesulfonamide | HCID 18760845 | 94% |
Reaction Steps
A mixture of 12.5 g of iron powder (223 mmol) and 16 mL of an aqueous solution of acetic acid (8%) was heated to 80° C., and a solution of 6 g of I -chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide (22.3 mmol) in 20 mL of glacial acetic acid and 22 mL ethyl acetate was added dropwise to the mixture. After heating for 1.5 h the reaction mixture was filtered through a pad of Celite® and washed with 200 mL of ethyl acetate and water (twice with 25 mL). The organic phase was separated, dried (MgSO4), filtered and concentrated under reduced pressure to yield 5 g (94%) of the title compound as a solid melting at 128-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06664400B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-bef168359c1344ba9cf349bd425414a3 |
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| Source note | uspto-grants-2003_12 |
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