HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428713Generated: October 30, 2026
Hydrochloric Acid → Ethyl 2-(4-(methylsulfonamidomethyl)phenyl)propanoate
https://huagongshe.com/reaction/1428713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 2-chloropropionate | HCID 10807 | — |
| Reactant | N-[(4-bromophenyl)methyl]methanesulfonamide | HCID 19027423 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Catalyst | Manganese | HCID 23930 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(4-(methylsulfonamidomethyl)phenyl)propanoate | HCID 70816013 | — |
Reaction Steps
To a stirred solution of N-(4-bromobenzyl)methanesulfonamide (675 mg, 2.555 mmol) in dimethylformamide were added ethyl 2-chloropropionate (0.42 mL), manganese (280 mg) and (2,2′-bipyridine)nickel(II)-dibromide (67 mg, 0.17885 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 removed in vacuo. The crude was purified by column chromatography to obtain ethyl 2-(4-(methylsulfonamidomethyl)phenyl)propanoate (325 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-416544318e194d2bb5f564fc25217aea |
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| Source note | uspto-grants-2015_01 |
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