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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411189Generated: November 3, 2026

Sodium Iodide → HCID 71252207, compound

https://huagongshe.com/reaction/2411189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantFuran, 2-(2-bromoethoxy)tetrahydro-HCID 11252558—
ReactantHCID 71253097HCID 71253097—
SolventDimethylformamideHCID 6228—
ProductHCID 71252207HCID 71252207—

Reaction Steps

Under a nitrogen stream, methyl 4-(1-ethoxycarbonylaminocyclopropyl)benzoate (430 mg) described in Preparation Example 67 was dissolved in a solution of tetrahydrofuran (10 mL) and N,N-dimethylformamide (5 mL), sodium hydride (72 mg) were added under ice-cooling, and the mixture was stirred for 15 min. Then, 2-(2-bromoethoxy)tetrahydrofuran (0.30 mL) and sodium iodide (catalytic amount) were added, and the mixture was stirred for 30 min under ice-cooling and at room temperature overnight. Furthermore, sodium hydride (72 mg) was added under ice-cooling, and the mixture was stirred for 15 min. 2-(2-Bromoethoxy)tetrahydrofuran (0.30 mL) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (129 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-4720c4ec34864b0a91f9260106bd9005
Source noteuspto-grants-2014_08