HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306483Generated: October 31, 2026
Potassium Carbonate → HCID 54298023, compound
https://huagongshe.com/reaction/2306483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 4298049 | HCID 4298049 | — |
| Reactant | HCID 18434103 | HCID 18434103 | — |
| Catalyst | Benzyltriethylammonium bromide | HCID 165294 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54298023 | HCID 54298023 | 97.8% |
Reaction Steps
A suspension of 10 g of (E)-[4-(4-bromo-but-2-enyloxy)-phenyl]-(4-bromo-phenyl)-methanone, 7.47 g of N-cyclopropyl-2,2,2-trifluoro-acetamide, 6.7 g of potassium carbonate and 0.55 g of benzyltriethylammonium bromide in 200 ml of acetonitrile is heated to boiling while stirring for 7 h. After cooling to room temperature the suspension is filtered. The filtrate is concentrated and the residue is dissolved in a mixture of 500 ml of melthylene chloride and 50 ml of methanol and stirred with 50 g of a strongly acidic and strongly basic ion exchanger, subsequently filtered and washed with methylene chloride to give two phases. The organic phase is dried and concentrated. 11.5 g of N-[4-[4-(4-bromo-benzoyl)-phenoxy]-but-2-enyl]-N-cyclopropyl-2,2,2-trifluoroacetamide are obtained as a yellowish solid, MS: m/e 412 (M+-CF3, 1Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06441177B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-2a96cf361498440183d2ab0b04e7d192 |
|---|
| Source note | uspto-grants-2002_08 |
|---|