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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369444Generated: November 1, 2026

Sodium Iodide → HCID 178506582, compound

https://huagongshe.com/reaction/1369444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHCID 178505331HCID 178505331—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
ProductHCID 178506582HCID 17850658286%

Reaction Steps

A solution of cis-3-benzyloxy-1-methanesulfonyloxycyclobutane (1.25 g, 4.8 mmol) and sodium iodide (2.16 g, 14.4 mmol) in dry acetone (20 ml) was refluxed under nitrogen for 3.5 days. The mixture was cooled and diluted with diethyl ether (150 ml). The suspension was filtered and the filtrate was concentrated. The residue was dissolved in ethyl acetate and filtered through a plug of silica gel, eluting with ethyl acetate to give trans-3-benzyloxy-1-iodocyclobutane (1.19 g, 86%) as an orange oil; 1H NMR (250 MHz, CDCl3) δ2.54-2.65 (2H, m), 2.94-3.04 (2H, m), 3.85-4.06 (2H, m), 4.40 (2H, s), 7.26-7.38 (5H1 m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579875B1
Source datasetuspto-grants-2003_06
ORD IDord-88a9aceb89a44f6d9f7da0692bde6a2a
Source noteuspto-grants-2003_06