HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chlorobenzoic Acid → 4-Cyano-4'-glycidylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chlorobenzoic Acid | HCID 447 | — |
| 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-chlorobenzoic acid was added to a reaction mixture obtained by dissolving 19 g of 4-allyloxy-4′-cyanobiphenyl in 150 mL of methylene chloride as divided into several times, and the mixture was stirred at room temperature for 24 hours. Insoluble matters thus deposited were removed by filtration, and water was added thereto. After separating the mixture, the organic layer was washed with a saturated aqueous solution of sodium hydrosulfite and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain a residue, which was purified by silica gel column chromatography and then subjected to recrystallization from ethanol to obtain 13 g of 4-cyano-4′-glycidylbiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07527746B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-d38a5b3c246a4e6b9a13ec61341175c7 |
| Source note | uspto-grants-2009_05 |