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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426186Generated: October 30, 2026

(5-Ethyl-2,6-dimethoxy-pyrimidin-4-yl)-(3-hydroxymethyl-5-methyl-phenyl)-methanone → 3-(5-Ethyl-2,6-dimethoxy-pyrimidine-4-carbonyl)-5-methyl-benzaldehyde

https://huagongshe.com/reaction/426186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Ethyl-2,6-dimethoxy-pyrimidin-4-yl)-(3-hydroxymethyl-5-methyl-phenyl)-methanoneHCID 59184675—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product3-(5-Ethyl-2,6-dimethoxy-pyrimidine-4-carbonyl)-5-methyl-benzaldehydeHCID 5918483067.4%

Reaction Steps

A mixture of (5-ethyl-2,6-dimethoxy-pyrimidin-4-yl)-(3-hydroxymethyl-5-methyl-phenyl)-methanone (4.8 g, 15.2 mmol) and manganese dioxide (13.2 g, 152 mmol) in dichloromethane (110 ml) was stirred for 48 hr. at room temperature. The mixture was filtered through celite pad and the pad was washed with dichloromethane. The combined filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography (eluent, EA:hexanes (1:4)) to afford 3.22 g (67%) a white solid. m.p. 89-91° C.; 1H NMR (200 MHz, CDCl3) δ 1.07 (3H, t, J=7.4 Hz), 2.41-2.52 (5H, m), 3.92 (3H, s), 4.06 (3H, s), 7.91 (1H, s), 7.99 (1H, s), 8.10 (1H, s), 10.01 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106064B2
Source datasetuspto-grants-2012_01
ORD IDord-5655953009694a26887cdddf2022cdcf
Source noteuspto-grants-2012_01