HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-(3-Acetylaminophenyl)-6-(3-pyridyl)hex-5-enoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (4-Carboxybutyl)triphenylphosphonium bromide | HCID 161236 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 53837382 | HCID 53837382 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(3-Acetylaminophenyl)-6-(3-pyridyl)hex-5-enoic acid | HCID 53792000 | — |
Reaction Steps
To a mixture of 217 g of 4-carboxybutyl-triphenylphosphonium bromide and 154 g of potassium tert.butoxide in 1.8 liters of tetrahydrofuran are added, at -25° C., 94 g of 3-acetylaminophenyl-3-pyridyl ketone. After 2 hours stirring at ambient temperature the reaction mixture is combined with 200 ml of water and then substantially evaporated down. The residue is taken up in 500 ml of water and washed with ethyl acetate. The aqueous phase is then neutralised by the addition of citric acid and extracted with ethyl acetate. The organic phase is evaporated down and the residue is recrystallised from ethyl acetate/acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05482948 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-0bc1f5315ad34ca48e606dd262ce8542 |
| Source note | uspto-grants-1996_01 |