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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377435Generated: October 30, 2026

Diethyl Ether → (3-Bromo-phenyl)-cyclopropyl-methyl-amine

https://huagongshe.com/reaction/2377435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthyl AcetateHCID 8857—
ReactantN-(3-Bromo-phenyl)-N-methyl-formamideHCID 12030886—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(3-Bromo-phenyl)-cyclopropyl-methyl-amineHCID 2110715415%

Reaction Steps

A stirred, cooled (0° C.) solution of N-(3-bromo-phenyl)-N-methyl-formamide (Intermediate 112, 2.6 g, 9.7 mmol) and titanium tetra-iso-propoxide (3.9 mL, 10.67 mmol) in tetrahydrofuran (40 mL) was treated with a 3M solution of ethyl magnesium bromide in ether (8.08 mL, 24.25 mmol) under argon and the resulting reaction mixture was allowed to warm to ambient temperature gradually and refluxed at 55° C. overnight. It was then cooled in an ice-bath, quenched with saturated aqueous ammonium chloride solution, filtered over celite and the aqueous phase was extracted with diethyl ether. The organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford an oil. Flash column chromatography over silica gel (230-400 mesh) using 1.5% ethyl acetate in hexane as the eluent afforded the title compound (0.321 g, 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468391B2
Source datasetuspto-grants-2008_12
ORD IDord-c2f37b4cc9d840ad8f9aae26b30a7944
Source noteuspto-grants-2008_12