HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Biphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | N-(Ethoxycarbonyl)alanine | HCID 10558934 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Biphenyl | HCID 7095 | — |
Reaction Steps
The techniques which resulted in successful amido acylation of benzene using phenyllithium were next applied to the Grignard reaction. N-ethoxycarbonylalanine was treated with 300 mol percent of phenylmagnesium bromide at -78° C. and allowed to warm to room temperature. The desired ketone was not observed. Several hours of refluxing in ether and tetrahydrofuran yielded biphenyl and starting material which was optically intact.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618710 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-e20e9e964f654740b22c0176b22e7cf0 |
| Source note | uspto-grants-1986_10 |