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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609940Generated: November 1, 2026

Methyl iodide → HCID 23590029, compound

https://huagongshe.com/reaction/1609940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 135617795HCID 135617795—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
ProductHCID 23590029HCID 2359002925%

Reaction Steps

A solution of 2-(4-{2-[2-(4-hydroxy-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-phenoxy)-2-methyl-propionic acid ethyl ester (0.15 g, 0.352 mmol), methyl iodide (0.15 g, 1.06 mmol), tetrabutylammonium bromide (0.023 g, 0.0713) mmol) in CH2Cl2 (8 mL) was treated with a 50% weight solution of NaOH (0.1 mL), and stirred at room temperature. The reaction mixture was extracted with water and more CH2Cl2 and the organic layer dried (MgSO4). The solvent was removed in vacuo to give a crude oil which was purified by flash chromatography (2/1 hexanes/EtOAc) to afford 0.038 g (25%) 2-(4-{2-[2-(4-methoxy-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-phenoxy)-2-methyl-propionic acid ethyl ester. 1H NMR (500 MHz, CDCl3) δ 7.87-7.85 (m, 2), 6.90-6.88 (m, 2H), 6.78-6.71 (m, 4H), 4.21-4.06 (m, 4H), 3.80 (s, 3H), 2.88 (t, 2H, J=6.60 Hz), 2.29 (s, 3H), 1.47 (s, 6H), 1.23 (t, 3H, J=7.33 Hz); MS (ES+) Calc'd for C25H30NO6: Found m/e 440 (M+1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982278B2
Source datasetuspto-grants-2006_01
ORD IDord-36389551a9e240de976724563758667e
Source noteuspto-grants-2006_01