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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192739Generated: October 30, 2026

3-Phenylphenol → 2-{[([1,1'-Biphenyl]-3-yl)oxy]methyl}oxirane

https://huagongshe.com/reaction/2192739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenylphenolHCID 11381—
ReactantPotassium CarbonateHCID 11430—
ReactantEpibromohydrinHCID 18430—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-{[([1,1'-Biphenyl]-3-yl)oxy]methyl}oxiraneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329773B2
Source datasetuspto-grants-2012_12
ORD IDord-a0165680b1834be0b587e28f453c51d6
Source noteuspto-grants-2012_12