Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290956Generated: October 29, 2026

Benzene → Biphenyl

https://huagongshe.com/reaction/2290956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantN-(Ethoxycarbonyl)alanineHCID 10558934—
ReactantHCID 178418255HCID 178418255—
ReactantHCID 178506676HCID 178506676—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductBiphenylHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618710
Source datasetuspto-grants-1986_10
ORD IDord-e20e9e964f654740b22c0176b22e7cf0
Source noteuspto-grants-1986_10