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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22126265 | HCID 22126265 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Iodo-4-phenoxybut-2-yne | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670465 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-15b486ed5b37459fb030d4a3a355249f |
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| Source note | uspto-grants-1987_06 |
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