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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244677Generated: November 1, 2026

Iodoethane → HCID 58826421, compound

https://huagongshe.com/reaction/2244677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHCID 86611033HCID 86611033—
SolventAcetonitrile tetrahydrofuranHCID 22177404—
ProductHCID 58826421HCID 58826421—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of (1R,3S,4S)-3-azido-4-hydroxy-cyclopentanecarboxylic acid methyl ester (500 mg) at r.t. in acetonitrile/THF 3:1 (8 ml) under an argon atmosphere were added Ag2O (1.88 g) and ethyl iodide (2.18 ml). The black suspension was stirred for 18 h at 60° C., then cooled to r.t. The black solid was filtered off and washed with ethyl acetate. The filtrate was concentrated. The crude product was purified by column chromatography (silica gel; gradient: cyclohexane→cyclohexane/EtOAc 7:3) to give (1R,3S,4S)-3-azido-4-ethoxy-cyclopentanecarboxylic acid methyl ester (474 mg) as light yellow oil. MS: 214.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678917B2
Source datasetuspto-grants-2010_03
ORD IDord-2a4ead4b08694488be25baf820fee935
Source noteuspto-grants-2010_03