HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Carboxybutyl)triphenylphosphonium bromide → HCID 54557606, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Carboxybutyl)triphenylphosphonium bromide | HCID 161236 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 67745971 | HCID 67745971 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54557606 | HCID 54557606 | — |
Reaction Steps
To a suspension of 307 g of 4-carboxybutyltriphenylphosphonium bromide and 233 g of potassium tert.butoxide in 2.8 liters of tetrahydrofuran are added, at -40° C., 140 g of 4-acetylaminophenyl-3-pyridyl-ketone and this mixture is stirred for 2 hours. The reaction mixture is decomposed by the addition of ice water and evaporated down. The residue is taken up in water and washed with ethyl acetate. The aqueous phase is acidified to pH 5 to 6 and extracted with ethyl acetate. The organic phase is concentrated by evaporation and the residue is recrystallised from ethyl acetate/diisopropylether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05482948 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-b540687b52e4443e827dd1fa1c729479 |
| Source note | uspto-grants-1996_01 |