Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19007818 | HCID 19007818 | 53.1% |
Reaction Steps
Into a reaction flask fitted with a stirrer, a thermometer, a nitrogen gas inlet tube and a reflux condenser, were placed 24.140 parts of p-hydroxybiphenyl, 51.120 parts of deionized water, 6.427 parts of NaOH and 0.127 part of tetrabutylammonium bromide and to this mixture, 18.161 parts of propargyl bromide was added dropwise and reacted at 80° C. for 6 hours. After completion of the reaction, the content was treated with an aqueous NaOH solution and then subjected to a fractionation with ethyl acetate. Thereafter, magnesium sulfate was added and the mixture was kept standing overnight to effect dehydration. After filtering off magnesium sulfate, the solvent was removed off by an evaporator and the residue was subjected to a column chromatography (silica gel 200 mesh) to obtain a purified 1-propargyloxybiphenyl. Yield 53.1%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05340931 |
|---|
| Source dataset | uspto-grants-1994_08 |
|---|
| ORD ID | ord-cd798c18164a4ca491e229aa683269ae |
|---|
| Source note | uspto-grants-1994_08 |
|---|