HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255341Generated: October 29, 2026
Acetamide → N-(3-bromo-5-fluorophenyl)acetamide
https://huagongshe.com/reaction/255341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamide | HCID 178 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,3-Dibromo-5-fluorobenzene | HCID 137003 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-bromo-5-fluorophenyl)acetamide | HCID 66774623 | 44% |
Reaction Steps
A mixture of acetamide (2.8 g, 47.2 mmol), palladium acetate (0.50 g, 0.80 mmol), XANTPHOS (0.68 g, 1.2 mmol) and cesium carbonate (18 g, 55.2 mmol) was degassed and purged with nitrogen twice. Dry dioxane (50 mL) was added followed by 1,3-dibromo-5-fluorobenzene (10 g, 39.4 mmol). The reaction was heated to 105° C. overnight and then allowed to cool to room temperature. Dichloromethane was added and the mixture was stirred vigorously for 1 hr. The mixture was filtered. The filtrate was concentrated to dryness. Chromatography on silica gel with 25% ethyl acetate in hexanes gave 4.0 g (44%) of the product as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07875715B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-287e818319a443658a9c9e6defe68ec8 |
|---|
| Source note | uspto-grants-2011_01 |
|---|