HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46453Generated: October 26, 2026
Bromobenzene → 1-Benzhydryl-2-benzimidoylazetidine
https://huagongshe.com/reaction/46453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Benzhydrylazetidine-2-carbonitrile | HCID 19772072 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzhydryl-2-benzimidoylazetidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04173566 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-201f8ce040b945188807dda424eff77c |
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| Source note | uspto-grants-1979_11 |
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