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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652118Generated: October 27, 2026

Sodium Iodide → 1-Iodo-4-phenoxybut-2-yne

https://huagongshe.com/reaction/652118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethanesulfonateHCID 85257—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22126265HCID 22126265—
SolventAcetoneHCID 180—
Product1-Iodo-4-phenoxybut-2-yneHCID 19849461—

Reaction Steps

By following the esterification method of part B of this preparation, the preceding compound was converted into 4-phenoxybut-2-yn-1-ol methanesulfonate in almost quantitative yield. The foregoing crude mesylate was dissolved in 15 ml of acetone and treated with a solution of 5.55 g (0.037 mol) of sodium iodide and 1.049 g (0.0123 mol) of sodium bicarbonate in 30 ml of acetone. The reaction mixture was stirred for 1 hour at room temperature and then the solvent was removed under reduced pressure. The residue was diluted with water and extracted with methylene chloride; the organic extracts were dried and evaporated. The residue was purified by silica gel column chromatography using hexane-ethyl acetate (95:5) as eluant, to yield 1-iodo-4-phenoxybut-2-yne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670465
Source datasetuspto-grants-1987_06
ORD IDord-15b486ed5b37459fb030d4a3a355249f
Source noteuspto-grants-1987_06