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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378320Generated: October 31, 2026

(3-Benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanol → (3-Benzyloxyphenyl)-(3,5-dimethoxyphenyl)methanone

https://huagongshe.com/reaction/2378320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanolHCID 69204493—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product(3-Benzyloxyphenyl)-(3,5-dimethoxyphenyl)methanoneHCID 6920305993.1%

Reaction Steps

To a stirred solution of (3-benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanol (11.51 g, 32.9 mmol) in CH2Cl2 (30 mL) at room temperature was added activated MnO2 powder (13.28 g, 153 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 (3-benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanone as a clear oil (10.67 g, 93% yield): 1H NMR (CDCl3) δ 3.82 (s, 6H, OCH3), 5.11 (s, 2H, CH2), 6.67 (t, J=2 Hz, 1H, Ar), 6.92 (d, J=2 Hz, 2H, Ar), 7.17-7.22 (m, 1H, Ar), 7.33-7.45 (m, 8H, Ar). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470723B2
Source datasetuspto-grants-2008_12
ORD IDord-75cab3d8fe4b4749b6f9337804f5df78
Source noteuspto-grants-2008_12