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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352482Generated: November 2, 2026

Iodoethane → HCID 68644205, compound

https://huagongshe.com/reaction/1352482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantN-(tert-Butoxycarbonyl)-D-prolinolHCID 688279—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68644205HCID 6864420535.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium hydride (60% purity, 4.6 g) was suspended in tetrahydrofuran (50 mL) and a solution (50 mL) of (R)-1-tert-butoxycarbonyl-2-hydroxymethylpyrrolidine (20 g) in tetrahydrofuran was added dropwise under ice-cooling. After the completion of the dropwise addition, the mixture was stirred with heating at 50° C. for 30 min and ice-cooled. Ethyl iodide (18.7 g) was added to the reaction mixture and the mixture was stirred overnight at room temperature. After the completion of the reaction, the solvent was concentrated and water was added to the obtained residue. The mixture was extracted with chloroform and dried over magnesium sulfate. The solvent was concentrated and the obtained residue was purified by silica gel column chromatography. The fraction eluted with hexane:ethyl acetate=3:1 was concentrated to give (R)-1-tert-butoxycarbonyl-2-ethoxymethylpyrrolidine (8.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220759B2
Source datasetuspto-grants-2007_05
ORD IDord-43fa6f20bc264d71924a45b5adca11a1
Source noteuspto-grants-2007_05