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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869018Generated: October 30, 2026

Ethyl 2-iodo-3-methylbenzoate → Ethyl 3-methyl-2-(oxazol-2-yl)benzoate

https://huagongshe.com/reaction/869018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-iodo-3-methylbenzoateHCID 12140519—
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 3-methyl-2-(oxazol-2-yl)benzoateHCID 904122672,057.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

In a microwave vial was dissolved ethyl 2-iodo-3-methylbenzoate (627 mg, 2.16 mmol) and 2-(tributylstannyl)oxazole (0.54 mL, 0.07 mmol) in DME (2.59 mL). The solution was degassed with N2 for 5 minutes then CuI (21 mg, 0.11 mmol) and Pd(PPh3)4 (125 mg, 0.11 mmol) were added. The reaction was purged with N2 and heated at 150° C. for 1 h. The reaction was cooled to room temperature, filtered through a pad of Celite and purified via silica gel chromatography (0-40% EtOAc in hexanes) to give the title compound of step A (333 mg, 67%). MS (ESI) mass calcd. for C13H13NO3, 231.1. m/z found 232.1 [M+H]+. 1H NMR (500 MHz, Chloroform-d) δ 7.89-7.82 (m, 1H), 7.79 (d, J=0.8 Hz, 1H), 7.48-7.43 (m, 2H), 7.30 (d, J=0.9 Hz, 1H), 4.17 (q, J=7.1 Hz, 2H), 2.27 (s, 3H), 1.18 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969352B2
Source datasetuspto-grants-2015_03
ORD IDord-36d9eb1fda7f411eb216a2a6997beb0e
Source noteuspto-grants-2015_03