HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Triphenyl[3-(3,4,5-trimethoxyphenyl)propyl]phosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-(3-Bromopropyl)-1,2,3-trimethoxybenzene | HCID 22609611 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Triphenyl[3-(3,4,5-trimethoxyphenyl)propyl]phosphonium bromide | HCID 19020969 | 51% |
Reaction Steps
Dissolved in 50 ml of toluene were 7.65 g (26.5 mmol) of 5-(3-bromopropyl)-1,2,3-trimethoxybenzene and 6.9 g (26.5 mmol) of triphenylphosphine, followed by heating under reflux for 23 hours. The reaction mixture was allowed to cool down to room temperature. The supernatant was thereafter removed by decantation, whereby 7.46 g of crude triphenyl[3-(3,4,5-trimethoxyphenyl)propyl]phosphonium bromide were obtained as colorless oil (yield: 51%). The crude oil was used in the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05321135 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-8850c8388fe348f0bd51a5abf843c299 |
| Source note | uspto-grants-1994_06 |