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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46453Generated: October 26, 2026

Bromobenzene → 1-Benzhydryl-2-benzimidoylazetidine

https://huagongshe.com/reaction/46453

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 numberUS04173566
Source datasetuspto-grants-1979_11
ORD IDord-201f8ce040b945188807dda424eff77c
Source noteuspto-grants-1979_11