HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 4-Cyano-4'-glycidylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-(4-Prop-2-enoxyphenyl)benzonitrile | HCID 2341987 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyano-4'-glycidylbiphenyl | HCID 59790561 | 68.4% |
Reaction Steps
20 g of m-chloroperbenzoic acid divided into portions was added in a few times to a solution prepared by dissolving 19 g of 4-allyloxy-4′-cyanobiphenyl in 150 ml of methylene chloride, and stirred at room temperature for 24 hours. The deposited insoluble was filtered away, water was added to it for liquid-liquid separation, and the organic layer was washed with an aqueous saturated sodium hydrosulfite solution and then dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the residue was purified through silica gel column chromatography and further recrystallized from ethanol to obtain 13 g of 4-cyano-4′-glycidylbiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07541071B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-183c3f584f464b6e83bcfeb80409b4b2 |
| Source note | uspto-grants-2009_06 |