HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-[(3-Phenoxyphenyl)methyl]pyridin-1-ium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| Reactant | HCID 70567605 | HCID 70567605 | — |
| Product | 1-[(3-Phenoxyphenyl)methyl]pyridin-1-ium bromide | HCID 21522963 | — |
Reaction Steps
52.6 g of the brominated product of m-tolylphenyl ether containing 26.3 g of 3-phenoxybenzyl bromide was added to a mixed solution of 100 ml of xylene and 50 ml of water, and then 11.9 g of pyridine was added thereto. The mixture was heated to 70° to 75°C, kept at the same temperature for 3 hours while stirring and then cooled to room temperature (about 20° - 30°C). The lower aqueous layer which separated was removed, washed with a small amount of xylene, evaporated and then dried under a reduced pressure to obtain 34.5 g of colorless, crystalline 3-phenoxybenzyl pyridinium bromide (m.p. 120° - 121°C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969393 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-915e94ed747349f0bd38ae61259ada56 |
| Source note | uspto-grants-1976_07 |