HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 131724323, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Ethynylphenol | HCID 32758 | — |
| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Reactant | HCID 23504263 | HCID 23504263 | — |
| Reactant | {[(Prop-1-en-1-yl)oxy]methyl}benzene | HCID 54218220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131724323 | HCID 131724323 | — |
Reaction Steps
In 48 g of tetrahydrofuran was dissolved 12 g of poly(p-hydroxystyrene) having a weight average molecular weight (Mw) of 9,000 and a dispersity (Mw/Mn) of 1.05. A catalytic amount of p-toluenesulfonic acid was added. At 10° C., 4.3 g (0.029 mol) of benzyl propenyl ether was added to the solution, which was stirred for 2 hours. The reaction mixture was precipitated from a water/isopropanol mixture, followed by filtration and drying. The end polymer was obtained in an amount of 13.5 g. On 1H-NMR analysis, the ratio of p-(1-benzyloxypropyl)oxystyrene units to p-hydroxystyrene units was approximately 22.5:77.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06682869B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-4d38b308faf3456bac818294cccbc6c6 |
| Source note | uspto-grants-2004_01 |