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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45439Generated: October 29, 2026

(2-(Benzyloxy)-3-tert-butylphenyl)(3-(pyridin-2-yl)phenyl)methanol → (2-(Benzyloxy)-3-tert-butylphenyl)(3-(pyridin-2-yl)phenyl)methanone

https://huagongshe.com/reaction/45439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(Benzyloxy)-3-tert-butylphenyl)(3-(pyridin-2-yl)phenyl)methanolHCID 58238562—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product(2-(Benzyloxy)-3-tert-butylphenyl)(3-(pyridin-2-yl)phenyl)methanoneHCID 58238568—

Reaction Steps

A solution of crude 3 (10.25 mmol) in dichloromethane (160 mL) was treated with manganese dioxide (14 g, 15 equiv.) and this suspension was stirred under reflux for 6 hr. The reaction mixture was filtered through Celite and the filter cake was washed with ethyl acetate. The solvent was removed on a rotary evaporator and the crude product was purified by chromatography on silica (110 g) with 5% ethyl acetate in heptane (5 L) to produce 4 (2.75 g, 64% over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541522B2
Source datasetuspto-grants-2013_09
ORD IDord-6d9c85febd71411d978afb7779d446c3
Source noteuspto-grants-2013_09