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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699427Generated: October 31, 2026

Methyl 4-iodosalicylate → HCID 22592609, compound

https://huagongshe.com/reaction/1699427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-iodosalicylateHCID 11380407—
ReactantHCID 22592650HCID 22592650—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 22592609HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346546B1
Source datasetuspto-grants-2002_02
ORD IDord-0d73393b06b44a7f8203632a282dd488
Source noteuspto-grants-2002_02