HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699427Generated: October 31, 2026
Methyl 4-iodosalicylate → HCID 22592609, compound
https://huagongshe.com/reaction/1699427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-iodosalicylate | HCID 11380407 | — |
| Reactant | HCID 22592650 | HCID 22592650 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22592609 | HCID 22592609 | — |
Reaction Steps
670 mg (3.1 mmol) of 3-(4,4-dimethylthiochroman-8-yl)prop-1-yne, 860 mg (3.1 mmol) of methyl 2-hydroxy-4-iodobenzoate and 33 ml of triethylamine are introduced into a three-necked flask under argon. The reaction mixture is degassed by sparging with nitrogen, 174 mg (0.25 mmol) of bis(triphenylphosphine)palladium(II) chloride and 71 mg of copper iodide are introduced and the reaction mixture is stirred at room temperature for eight. hours. The reaction mixture is evaporated to dryness, the residue is taken up in ethyl acetate and hydrochloric acid (1N) and the organic phase is separated by settling, dried over magnesium sulphate and evaporated. The residue is purified by chromatography on a silica column eluted with a mixture composed of 99% heptane and 1% ethyl acetate. After evaporating the solvents, 1.50 g (75%) of methyl 2-hydroxy-4-[3-(4,4-dimethylthiochroman-8-yl)prop-1-yn-yl]benzoate are collected in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06346546B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-0d73393b06b44a7f8203632a282dd488 |
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| Source note | uspto-grants-2002_02 |
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