HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylphenol → 2-{[([1,1'-Biphenyl]-3-yl)oxy]methyl}oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylphenol | HCID 11381 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-{[([1,1'-Biphenyl]-3-yl)oxy]methyl}oxirane | HCID 14796822 | — |
Reaction Steps
4.7 g of m-phenylphenol, 15.1 g of epibromohydrin, 13.6 g of potassium carbonate and 33.3 g of 2-butanone were introduced into a three-necked flask with reflux condenser and stirrer. In addition, air was slowly passed through and the temperature was held at 70° C., and the mixture was stirred for 15 hours. After filtration, the filtrate was freed from low-boiling components in a rotary evaporator. m-Phenylphenol glycidyl ether was obtained as a clear, liquid product: 1H-NMR (CDCl3, 400 MHz): 2.78 (dd, 1H), 2.90 (t, 1H), 3.36 (m, 1H), 4.02 (dd, 1H), 4.24 (dd, 1H), 6.90 (dd, 1H), 7.15 (d, 1H), 7.20 (d, 1H), 7.35 (m, 2H), 7.40 (t, 2H), 7.55 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329773B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-a0165680b1834be0b587e28f453c51d6 |
| Source note | uspto-grants-2012_12 |