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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13774Generated: October 29, 2026

Iodoethane → (S)-1-(benzyloxycarbonyl)-3-(N,N-diethylamino)pyrrolidine

https://huagongshe.com/reaction/13774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-1-Cbz-3-AminopyrrolidineHCID 1519355—
Product(S)-1-(benzyloxycarbonyl)-3-(N,N-diethylamino)pyrrolidineHCID 68693001—

Reaction Steps

To a solution of 1.40 g of (S)-3-amino-1-(benzyloxycarbonyl)pyrrolidine (J. Med. Chem., 1992, 35, 1764-1773) in 28 ml of tetrahydrofuran, 2.6 g of potassium carbonate and 1.0 ml of ethyl iodide were added under ice-cool stirring, followed by stirring for 24 hours. The reaction solution was concentrated under reduced pressure, mixed with water, followed by extraction with ethyl acetate, and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 0.70 g of the objective compound as a yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728131B2
Source datasetuspto-grants-2010_06
ORD IDord-2f4d393ee06c4c96bd870b37c357c585
Source noteuspto-grants-2010_06