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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042511Generated: November 2, 2026

(2-(Benzyloxy)biphenyl-3-yl)(2-methoxybiphenyl-3-yl)methanol → (2-(Benzyloxy)biphenyl-3-yl)(2-methoxybiphenyl-3-yl)methanone

https://huagongshe.com/reaction/1042511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(Benzyloxy)biphenyl-3-yl)(2-methoxybiphenyl-3-yl)methanolHCID 58238521—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product(2-(Benzyloxy)biphenyl-3-yl)(2-methoxybiphenyl-3-yl)methanoneHCID 5823852262%

Reaction Steps

A solution of crude 3 (3.46 mmol) in dichloromethane (60 mL) was treated with manganese dioxide (85%, 5.3 g, 15 equiv) and this suspension was stirred at reflux overnight. The solids were filtered out and washed with ethyl acetate. The solvent was removed in a rotary evaporator and the residue was chromatographed on silica (85 g) with 2% ethyl acetate in heptane (5 L). Pure 4 (0.48 g) as well as slightly impure 4 (1.01 g) were isolated (total yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557936B2
Source datasetuspto-grants-2013_10
ORD IDord-9d78099182e24def88e3ccc4d7b0ae5d
Source noteuspto-grants-2013_10