Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886501Generated: October 30, 2026

4-Phenoxyphenol → HCID 19876214, compound

https://huagongshe.com/reaction/1886501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxyphenolHCID 13254—
Reactant4-NitrobenzilHCID 283893—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 19876214HCID 19876214—

Reaction Steps

Equimolar amounts of 4-nitrobenzil and 4-phenoxyphenol are reacted in the presence of potassium t-butoxide under conditions described in Example 56 paragraph (d) to form 4-(phenoxyphenoxy)benzil. A polyquinoxaline terminated by aromatic groups which are susceptible to aromatic electrophilic substitution is synthesized by the reaction of p-BOB from Example 56, -(phenoxyphenoxy)benzil and 3,3',4,4'-tetraaminobiphenyl in m-cresol The resulting polyquinoxaline polymer is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151489
Source datasetuspto-grants-1992_09
ORD IDord-d1e14127cdef49ca870e97ab2cd41405
Source noteuspto-grants-1992_09