HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4'-Bromo-4-carboxymethylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1-(4'-Bromo(1,1'-biphenyl)-4-yl)ethan-1-one | HCID 79806 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Product | 4'-Bromo-4-carboxymethylbiphenyl | HCID 1394245 | — |
Reaction Steps
The compound (3 g) obtained in the above (1) is suspended in morpholine (20 ml), and thereto is added sulfur (0.71 g), and the mixture is refluxed with stirring for five hours. After cooling, the reaction mixture is poured into water, and extracted with ethyl acetate. The organic layer is washed with 1N hydrochloric acid (twice) and a saturated brine (twice), and dried over anhydrous sodium sulfate. The desiccant is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is suspended in ethanol, and the precipitates are collected by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048854 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-78e0cf40f386481aa4f06f0069be9b7d |
| Source note | uspto-grants-2000_04 |