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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230162Generated: November 3, 2026

[4-Chloro-2-(2-chloro-phenoxy)-pyrimidin-5-yl]-thiophen-2-yl-methanol → [4-Chloro-2-(2-chloro-phenoxy)-pyrimidin-5-yl]-thiophen-2-yl-methanone

https://huagongshe.com/reaction/230162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-Chloro-2-(2-chloro-phenoxy)-pyrimidin-5-yl]-thiophen-2-yl-methanolHCID 59834363—
CatalystManganese dioxideHCID 14801—
SolventTolueneHCID 1140—
Product[4-Chloro-2-(2-chloro-phenoxy)-pyrimidin-5-yl]-thiophen-2-yl-methanoneHCID 59834304—

Reaction Steps

[4-Chloro-2-(2-chloro-phenoxy)-pyrimidin-5-yl]-thiophen-2-yl-methanol (98 mg, 0.28 mmol)was dissolved in 15 mL dry toluene, and 250 mg of MnO2 was added. The reaction mixture was heated to reflux for 30 minutes, and water was removed using a Dean Stark apparatus. The hot reaction mixture was filtered through Celite, and the Celite was washed five times with 3.5 mL of hot EtOAc. The combined organics were evaporated under reduced pressure to yiled 82 mg of [4-Chloro-2-(2-chloro-phenoxy)-pyrimidin-5-yl]-thiophen-2-yl-methanone as an oil. Mass Spec. M+H=352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566708B2
Source datasetuspto-grants-2009_07
ORD IDord-5e1f49e4c4f6459eafe9e32944cc759b
Source noteuspto-grants-2009_07