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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377420Generated: November 2, 2026

Tetrahydrofuran → Cyclopropyl-methyl-(4-methyl-3-trimethylsilanylethynyl-benzyl)-amine

https://huagongshe.com/reaction/2377420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantBenzenemethanamine, 3-bromo-N-cyclopropyl-N,4-dimethyl-HCID 21107149—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductCyclopropyl-methyl-(4-methyl-3-trimethylsilanylethynyl-benzyl)-amineHCID 5742424894.1%

Reaction Steps

Following General Procedure D and using cyclopropyl-(3-bromo-4-methyl-benzyl)-methyl-amine (Intermediate 97, 2.24 g, 8.81 mmol), triethyl amine (10 mL), tetrahydrofuran (5 mL), copper(I)iodide (0.4 g, 2.1 mmol), trimethylsilyl acetylene (5 mL, 35.4 mmol) and dichlorobis(triphenylphosphine)palladium(II) (1.45 g, 2.06 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using 6-10% ethyl acetate in hexane as the eluent, the title compound (2.25 g, 94%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468391B2
Source datasetuspto-grants-2008_12
ORD IDord-31d97c8c837a4039a6af37aa0fa2bbea
Source noteuspto-grants-2008_12