Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048969Generated: October 30, 2026

Bromobenzene → 1-Benzhydryl-2-benzimidoylazetidine

https://huagongshe.com/reaction/2048969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantMagnesiumHCID 5462224—
Reactant1-Benzhydrylazetidine-2-carbonitrileHCID 19772072—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
Product1-Benzhydryl-2-benzimidoylazetidineHCID 20345301—

Reaction Steps

Suspend phenylmagnesium bromide in ether by adding under gentle reflux a solution of 189.2 g of bromobenzene in 500 ml of ether to a stirred suspension of 24.4 g of magnesium turnings in 1000 ml. of dry ether. Upon completion of the addition, reflux for another 30 minutes, then allow the mixture to cool for 15 minutes at room temperature. Add portionwise, over 3 to 4 minutes, 119.6 g of 1-benzhydryl-2-cyanoazetidine. Stir the mixture for 18 hours at room temperature, cool to 0° C. and quench by the sequential addition of 750 ml. of water, 250 ml. of ether and 400 ml. of methylene chloride. Filter the mixture. Remove the aqueous layer of the filtrate. Wash the organic phase with water and dry over anhydrous sodium sulfate. Remove the solvent in vacuo. Triturate the solid residue with 500 ml of isopropyl ether and filter to obtain the analytically pure title product, m.p. 123.5°-126.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04196124
Source datasetuspto-grants-1980_04
ORD IDord-95c27f5f353543acb846e65a58c425d1
Source noteuspto-grants-1980_04