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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695929Generated: October 27, 2026

(2-(2-(Piperidin-1-yl)ethylamino)-3-fluorophenyl)methanol → 2-(2-(Piperidin-1-yl)ethylamino)-3-fluorobenzaldehyde

https://huagongshe.com/reaction/1695929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(2-(Piperidin-1-yl)ethylamino)-3-fluorophenyl)methanolHCID 57774402—
CatalystManganese dioxideHCID 14801—
SolventTolueneHCID 1140—
Product2-(2-(Piperidin-1-yl)ethylamino)-3-fluorobenzaldehydeHCID 57774413—

Reaction Steps

(2-(2-(piperidin-1-yl)ethylamino)-3-fluorophenyl)methanol (453 mg, 1.795 mmol) and MnO2 (692 mg, 7.960 mmol) were heated in toluene (15 mL) at reflux overnight. The suspension was filtered through Celite with CH2Cl2 and concentrated on a rotary evaporator. Crude 2-(2-(piperidin-1-yl)ethylamino)-3-fluorobenzaldehyde was carried on to the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-86435a16b620414f925a41ddab357764
Source noteuspto-grants-2012_04