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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047901Generated: October 31, 2026

Ethyl 2-iodo-3-methylbenzoate → HCID 59314297, compound

https://huagongshe.com/reaction/1047901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-iodo-3-methylbenzoateHCID 12140519—
Reactant4,4,5,5-Tetramethyl-2-(2-methylprop-1-en-1-yl)-1,3,2-dioxaborolaneHCID 15148447—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59314297HCID 5931429785%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of the 2-iodo-3-methylbenzoic acid ethyl ester (289) (2.9 g-0.01 mol) and 2-methyl-1-propenylboronic acid pinacol ester (3.64 g-0.02 mol-2 eq) in dry DMF (50 mL) and saturated NaHCO3 (10 mL) is degassed for 10 minutes and then treated with tetrakis(triphenylphosphine)palladium(0) (400 mg). The mixture is stirred at 110° C. overnight. The reaction is cooled and the DMF removed in vacuo and the residue diluted with water (120 mL). The aqueous is filtered through hyflo and extracted with EtOAc (3×75 mL). The organic extracts are washed with water (2×50 mL) and brine (2×50 mL), and dried over MgSO4. The organic extracts are concentrated in vacuo and purified by flash chromatography (400 g silica gel, 5% EtOAc in heptane) to give the product as pale yellow oil (1.85 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-2c4490287a224d58a2d3cce732176a0f
Source noteuspto-grants-2013_10