HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (E)-1,4-Bis(-4-bromostyryl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Phosphonic acid, P,P'-(1,4-phenylenebis(methylene))bis-, P,P,P',P'-tetraethyl ester | HCID 78303 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (E)-1,4-Bis(-4-bromostyryl)benzene | HCID 12266563 | — |
Reaction Steps
50% aqueous sodium hydroxide (20 ml) was added to a solution of tetraethyl p-xylylenebisphosphonate (2.40 g, 6.35 mmol) (25) and 4-bromobenzaldehyde (2.41 g, 13.02 mmol) in 10 ml of benzene. Tetra-n-butylammonium iodide (148 mmg) was added and the mixture was refluxed under nitrogen for 1 hour. The reaction mixture was allowed to cool and diluted by the addition of water (25 ml). A yellow solid was collected and washed three times with water, methanol and ether. The product was purified by recrystallization from xylenes and was isolated in 61.9% (1.73 g) yield (Product is insoluble in standard solvents).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07459106B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-c9179945d71441d98244d7e77c38dd4d |
| Source note | uspto-grants-2008_12 |