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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377144Generated: November 1, 2026

Benzofuran-5-yl-(3-ethoxy-4-methoxy-phenyl)-methanol → Benzofuran-5-yl-(3-ethoxy-4-methoxy-phenyl)-methanone

https://huagongshe.com/reaction/2377144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzofuran-5-yl-(3-ethoxy-4-methoxy-phenyl)-methanolHCID 68936547—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductBenzofuran-5-yl-(3-ethoxy-4-methoxy-phenyl)-methanoneHCID 68941709—

Reaction Steps

To a stirred solution of benzofuran-5-yl-(3-ethoxy-4-methoxy-phenyl)-methanol (2.36 g crude, 6.8 mmol) in CH2Cl2 (15 mL) at room temperature was added activated MnO2 powder (6.0 g, 69 mmol) and kept adding 2˜3 equivalents of MnO2 every 3˜5 h until HPLC showed disappearance of the starting material. The black suspension was filtered through a Celite pad, concentrated in vacuo to give benzofuran-5-yl-(3-ethoxy-4-methoxy-phenyl)-methanone as an off-white solid (2.25 g, 111% crude yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468446B2
Source datasetuspto-grants-2008_12
ORD IDord-c59415a9ac684e10a8ce4478d7665065
Source noteuspto-grants-2008_12