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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384698Generated: October 30, 2026

Methyl iodide → 4-Methoxybenzo(d)oxazole

https://huagongshe.com/reaction/1384698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Benzoxazol-4-olHCID 13720697—
SolventAcetoneHCID 180—
Product4-Methoxybenzo(d)oxazoleHCID 2250093591%

Reaction Steps

To a suspension of 4-hydroxybenzoxazole (2.00 g, 14.8 mmol) (Musser et al., J. Med. Chem., 30, pp. 62-67 (1987)) in acetone (80.0 ml) was added dried K2CO3 (2.25 g, 16.3 mmol) followed by iodomethane (1.38 ml, 22.2 mmol). The reaction was heated under reflux under N2 for 4.5 h, then filtered and reduced in vacuo to afford the crude product. The resulting residue was purified by flash chromatography (25:75 ethyl acetate/hexane) to give 2.0 g (91%) of the title compound as a white crystalline solid: m.p. 72-74° C.; IR (KBr) 3089, 1619, 1610, 1503, 1496, 1322, 1275, 1090, 1071, 780, 741; 1H NMR (CDCl3) δ 8.02 (1H, s), 7.32 (1H, t, J=8.0), 7.18 (1H, d, J=8.0), 6.81 (1H, d, J=8.0), 4.04 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258948B1
Source datasetuspto-grants-2001_07
ORD IDord-8700c87177644d3f8eade2cc56f51067
Source noteuspto-grants-2001_07