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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34010Generated: October 26, 2026

(2-Chlorothiophen-3-yl)naphthalen-2-yl Methanol → (2-Chlorothiophen-3-yl)-(naphthalen-2-yl)-methanone

https://huagongshe.com/reaction/34010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chlorothiophen-3-yl)naphthalen-2-yl MethanolHCID 23070162—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product(2-Chlorothiophen-3-yl)-(naphthalen-2-yl)-methanoneHCID 2307019252.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1.18 g of (2-chlorothiophen-3-yl)-(naphthalen-2-yl)-methanol in 12 mL of toluene was added 1.12 g of activated manganese dioxide at room temperature, and after stirring at 50° C. for a day, manganese dioxide was filtered off through Celite. The solvent was distilled off, and the resultant crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:50), to afford 0.61 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-853adcebad0e4c17ad3678e7816250a7
Source noteuspto-grants-2008_09