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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-(3-Bromo-phenyl)-N-methyl-formamide | HCID 12030886 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (3-Bromo-phenyl)-cyclopropyl-methyl-amine | HCID 21107154 | 15% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468391B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-c2f37b4cc9d840ad8f9aae26b30a7944 |
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| Source note | uspto-grants-2008_12 |
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