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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592426Generated: November 1, 2026

[3-(1-Ethyl-1-methoxy-propyl)-pyridin-2-yl]-methanol → 3-(1-Ethyl-1-methoxy-propyl)-pyridine-2-carbaldehyde

https://huagongshe.com/reaction/1592426

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(1-Ethyl-1-methoxy-propyl)-pyridin-2-yl]-methanolHCID 67272374—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product3-(1-Ethyl-1-methoxy-propyl)-pyridine-2-carbaldehydeHCID 8659476046%

Reaction Steps

Activated MnO2 (0.458 g, 5.26 mmol) was added to a stirred solution of [3-(1-ethyl-1-methoxy-propyl)-pyridin-2-yl]-methanol (0.110 g, 0.526 mmolbin CH2Cl2 (3 mL). The mixture was stirred for 16 h, and then filtered through a celite cake. The filtrate was concentrated by evaporation under vacuum, and the residue was purified by flash chromatography on a silica gel column (CH2Cl2), affording 3-(1-ethyl-1-methoxy-propyl)-pyridine-2-carbaldehyde as yellow oil (0.086 g, 46%). 1H NMR (CDCl3) δ 0.71 (t, 6H, J=7.5 Hz), 1.83-2.09 (m, 4H) 3.16 (s, 3H), 7.37 (dd, 1H, J=7.7, 4.8 Hz), 7.62 (dd, 1H, J=7.8, 1.5 Hz), 8.65 (dd, 1H, J=4.8, 1.5 Hz), 10.57 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291631B2
Source datasetuspto-grants-2007_11
ORD IDord-3a225f3dd8744721b8ed9ad98025487f
Source noteuspto-grants-2007_11