Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882292Generated: October 30, 2026

Toluene → 4-Iodo-2-vinylphenol

https://huagongshe.com/reaction/1882292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-Hydroxy-4-iodobenzaldehydeHCID 18351513—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product4-Iodo-2-vinylphenolHCID 1610223898%

Reaction Conditions

Temperature23 °C

Reaction Steps

Haloorganic compound 15 was synthesized by a multi-step process. To a mixture of methyltriphenylphosphonium bromide (14.08 g, 39.4 mmol) in toluene at 23° C. was added a solution of potassium tert-butoxide (4.47 g, 39.8 mmol) in THF (60 mL) dropwise via cannula, and the resulting mixture was allowed to stir at 23° C. for 4 hours. The resulting yellow mixture was cooled to −78° C. and a solution of 4-iodo-salicylaldehyde (4.35 g, 17.5 mmol) in toluene (40 mL) was added dropwise via cannula. The resulting mixture was allowed to slowly warm to 23° C. and was stirred at that temperature for 12 hours. The reaction was then quenched with the addition of saturated aq. ammonium chloride (100 mL). The resulting mixture was then diluted with water (200 mL) and extracted with Et2O (3×100 mL). The combined organic fractions were then washed with brine (100 mL), dried over magnesium sulfate, and concentrated in vacuo. Purification by flash chromatography (SiO2, hexanes:ethyl acetate 7:1→1:1) yielded 2-hydroxy-5-iodostyrene as a colorless solid (4.0 g, 98%). See also Gligorich, K. M., 2006.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318983B2
Source datasetuspto-grants-2012_11
ORD IDord-28e7166b9ef34732a8ce3a604be2829e
Source noteuspto-grants-2012_11