HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842987Generated: October 31, 2026
Trifluoroacetic acid → 2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid
https://huagongshe.com/reaction/1842987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate | HCID 70816333 | — |
| Catalyst | Manganese | HCID 23930 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid | HCID 70816569 | — |
Reaction Steps
To a solution of ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate (305 mg, 1.03 mmol) in DMF, manganese (113 mg, 2.06 mmol), NiBr2bipy (27 mg, 0.07 mmol), ethyl-2-chloro propionate (0.17 mL, 1.34 mmol) was added, followed by addition of TFA (0.002 mL, 0.028 mmol). The mixture was stirred for 1 day at 65° C. The reaction mixture was quenched by conc. HCl (7-drops) and then extracted with diethyl ether, dried (MgSO4) and the solvent was evaporated in vacuo. The residue was purified by CC (EtOAc/n-hexane). 2-(4-(ethyl-sulfonamidomethyl)-3-fluorophenyl)propanoic acid in pure form (65 mg, 20%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946204B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-5a0a674743504fb2a83b21ff1159eeaf |
|---|
| Source note | uspto-grants-2015_02 |
|---|