HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428770Generated: November 1, 2026
Trifluoroacetic acid → Ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate
https://huagongshe.com/reaction/1428770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl 2-chloropropionate | HCID 10807 | — |
| Reactant | N-(4-bromo-2-fluorobenzyl)ethanesulfonamide | HCID 70816043 | — |
| Catalyst | Manganese | HCID 23930 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate | HCID 70816333 | — |
Reaction Steps
To a solution of N-(4-bromo-2-fluorobenzyl)ethanesulfonamide (305 mg, 1.03 mmol) in dimethylformamide, Manganese (113 mg, 2.06 mmol), (2,2′-Bipyridine)nickel(II)-dibromide (27 mg, 0.07 mmol), ethyl 2-chloropropanoate (0.17 mL, 1.34 mmol) was added. It was followed by addition of trifluoroacetic acid (0.002 mL, 0.028 mmol). The mixture was stirred for 24 h at 65° C. The reaction mixture was quenched by concentrated HCl (7 drops). Then it was extracted with diethyl ether, dried over magnesium sulfate, the solvent was evaporated in vacuo. It was purified by column chromatography to obtain ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate in pure form (65 mg, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937092B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-7edd26114cc04e33bfd956ab2d6f7af1 |
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| Source note | uspto-grants-2015_01 |
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