HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybiphenyl → 4,4'-Dihydroxybiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | 4-(4-Hydroxyphenyl)-3-cyclohexen-1-ol | HCID 14365708 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 4,4'-Dihydroxybiphenyl | HCID 7112 | — |
Reaction Steps
It was found that a novel compound 4-(4-hydroxyphenyl)-3-cyclohexene-1-ol can be obtained in good yield by conducting a decomposition reaction in the initial stage of a reaction in the absence of a dehydrogenation catalyst and a hydrogen acceptor, and that by-products such as p-phenylphenol can be virtually inhibited by conducting the dehydrogenation reaction of the novel compound to give 4,4'-biphenol of high purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04873374 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-2033ed781491465f900af013c7f2aaf5 |
| Source note | uspto-grants-1989_10 |