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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504295Generated: October 25, 2026

Phenylacetonitrile → 1-Benzylcyclopropylamine

https://huagongshe.com/reaction/1504295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetonitrileHCID 8794—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product1-BenzylcyclopropylamineHCID 152923—

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 etherate 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212348B2
Source datasetuspto-grants-2015_12
ORD IDord-be2f89d01baa49cb8be2ea8d5d834e92
Source noteuspto-grants-2015_12