HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754112Generated: October 28, 2026
Triethylamine → N-(4-((3-(trifluoromethoxy)phenyl)sulfonyl)phenyl)acetamide
https://huagongshe.com/reaction/1754112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) | HCID 2734385 | — |
| Reactant | Sodium 4-acetamidobenzene-1-sulfinate | HCID 23666794 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | N-(4-((3-(trifluoromethoxy)phenyl)sulfonyl)phenyl)acetamide | HCID 70978998 | 57.9% |
Reaction Steps
To a solution of sodium 4-acetamidobenzenesulfinate dehydrate (128 mg, 0.5 mmol), 3-trifluoromethoxy-phenylboronic acid (144 mg, 0.75 mmol) and Et3N (0.313 mL, 2.25 mmol) in 1,4-dioxane (4 mL) and DMSO (4 mL) is added Cu(OAc)2 (114 mg, 0.625 mmol). The mixture is heated at 60° C. for 16 h then cooled to ambient temperature. EtOAc (12 ml) and brine (6 ml) is added followed by concentrated NH4OH (0.6 mL) and the mixture is stirred at ambient temperature for 15 min. The layers are separated and the aqueous layer is extracted with EtOAc (6 mL). The combined extracts are dried (Na2SO4) and evaporated. The residue is purified by preparative TLC with 2:1 EtOAc/hexanes to give 104 mg (57%) white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09169209B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-8008021cc14c4081b4213b819b0bdec4 |
|---|
| Source note | uspto-grants-2015_10 |
|---|