Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092745Generated: November 1, 2026

Acetone → 5-Tert-butyloxazole-4-carboxaldehyde

https://huagongshe.com/reaction/1092745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant3-(5-tert-Butyloxazol-4-yl)-2-hydroxyacrylic acidHCID 66590043—
CatalystManganese dioxideHCID 14801—
Product5-Tert-butyloxazole-4-carboxaldehydeHCID 21031488—

Reaction Steps

To a solution of oxazole alcohol 3 (9.9 g, 64 mmol) in acetone (200 mL, Aldrich, Cat. No. 179124) was added MnO2 (27.7 g, 319 mmol, 5 equiv., Wako Pure Chemical, Osaka, Japan, Cat. No. 138-09675), and the mixture was stirred at room temperature overnight. After celite filtration to remove MnO2, the solvent was removed by evaporation, and the residual pale brown oil was dissolved in CHCl3 and applied to silica-gel column chromatography (prepared with CHCl3), then eluted with CHCl3:MeOH (100:1 to 50:1), to give an pale yellow oil of aldehyde 4 (5.54 g, 57% (38% in two steps)). Rf 0.65 (CHCl3:MeOH=10:0.5), 1H NMR (300 MHz CDCl3) δ 10.10 (s, 1H), 7.77 (s, 1H), 1.47 (s, 9H); HRMS (EI): m/z 153.0794 (M+) (Calcd for C8H11NO2: 153.0790).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129527B2
Source datasetuspto-grants-2012_03
ORD IDord-d420428afd6c4db9bfd7d3737c272aa2
Source noteuspto-grants-2012_03