HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428727Generated: November 2, 2026
Hydrochloric Acid → Ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate
https://huagongshe.com/reaction/1428727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 2-chloropropionate | HCID 10807 | — |
| Reactant | N-(4-bromo-2-fluorobenzyl)methanesulfonamide | HCID 70847718 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Catalyst | Manganese | HCID 23930 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate | HCID 70855559 | — |
Reaction Steps
To a stirred solution of N-(4-bromo-2-fluorobenzyl)methanesulfonamide (2.94 g, 10.421 mmol) in dimethylformamide were added ethyl 2-chloropropionate (1.725 mL), manganese (1.145 g) and (2,2′-bipyridine)nickel(II)-dibromide (273 mg, mmol). Trifluoroacetic acid (2 drops) was added. The reaction mixture was stirred for 36 h at 60° C. After cooling down to room temperature, the mixture was hydrolysed by 1N HCl and extracted with diethyl ether. The organic layer was dried over magnesium sulfate and filtered. The filtrate was removed in vacuo. The crude was purified by column chromatography to obtain ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate (218 mg).
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-9393fb64e4fb4ed1a590ce015091ef73 |
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| Source note | uspto-grants-2015_01 |
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