HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159060Generated: November 5, 2026
Potassium Acetate → N,N-diethyl-4-hydroxy-2-(trifluoromethoxy)benzamide
https://huagongshe.com/reaction/1159060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 4-bromo-N,N-diethyl-2-(trifluoromethoxy)benzamide | HCID 68687835 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-diethyl-4-hydroxy-2-(trifluoromethoxy)benzamide | HCID 68687198 | 82.5% |
Reaction Steps
To a stirring degassed solution of N,N-diethyl-4-bromo-2-(trifluoromethoxy)benzamide (2768 mg, 8.2 mmol), bis(pinacolato)diboron (2281 mg, 9.0 mmol), and potassium acetate (2402 mg, 24.5 mmol) in dry DMF (60 mL) was added palladium(II) acetate (55 mg, 0.25 mmol). The reaction was heated to 80° C. for 2 h and then cooled to room temp. The reaction was quenched with water and extracted with EtOAc (3×75 mL). The organic layers were combined, dried over Na2SO4, and conc. in vacuo to a brown oil. The oil was dissolved in THF (40 mL) and acetic acid (2.0 mL) and treated with hydrogen peroxide (8 mL). The reaction was stirred for 15 min and then quenched with st. aq. NaHSO3. The reaction was extracted with EtOAc (3×40 mL). The organic layers were combined, dried over Na2SO4, and conc. in vacuo to a brown oil. The oil was purified by flash chromatography (silica gel, 20-70% EtOAc in hexanes) to give 1876 mg of the desired product as a white solid. MS (ESI) 278 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07812024B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-a2281878d97d4255bc70dab15c0f2a72 |
|---|
| Source note | uspto-grants-2010_10 |
|---|