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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244956Generated: October 26, 2026

Phenylacetonitrile → 1-Benzylcyclopropylamine

https://huagongshe.com/reaction/244956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetonitrileHCID 8794—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product1-BenzylcyclopropylamineHCID 15292358.6%

Reaction Steps

4.5 g (38 mmol) of phenylacetonitrile was dissolved in 50 mL of tetrahydrofuran, mixed with 12.4 mL (41.9 mmol) of tetraisopropyl propylorthotitanate and 78 mL (76 mmol) of 0.98M ethylmagnesium bromide in tetrahydrofuran and stirred at room temperature for 1 hour. After the stirring, 9.6 mL (78 mmol) of boron trifluoride ethyl ether complex was added, and the reaction solution was stirred at room temperature for another 1 hour. After completion of the reaction, 2 M aqueous sodium hydroxide was added, and the reaction solution was extracted with diethyl ether. After addition of 3 M hydrochloric acid, the organic layer was separated. The resulting aqueous layer was basified with 5 M aqueous sodium hydroxide and extracted with methylene chloride. The solvent was removed from the organic layer under reduced pressure to give 3.28 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658686B2
Source datasetuspto-grants-2014_02
ORD IDord-5fa202b69a2543eea21c836f9ebaed9f
Source noteuspto-grants-2014_02