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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801592Generated: October 30, 2026

HCID 59803202, compound → HCID 59803209, compound

https://huagongshe.com/reaction/1801592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59803202HCID 59803202—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductHCID 59803209HCID 5980320976.3%

Reaction Steps

To a solution of methyl 1-(2-chloro-5-(hydroxymethyl)phenyl)piperidine-4-carboxylate 67 (0.198 g, 0.698 mmol) in DCM (3.5 mL) was added MnO2 (0.688 mg, 7.91 mmol). The reaction mixture was stirred at room temperature for 17 h, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluted with 10% to 40% EtOAc in hexanes) gave methyl 1-(2-chloro-5-formylphenyl)piperidine-4-carboxylate 68 (0.150 g, 76.3% yield) as a colorless oil. Mass spectrum: calculated for C14H16ClNO3 281.1. found 282.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349831B2
Source datasetuspto-grants-2013_01
ORD IDord-a3ed95b4635d459681e25f7b7d1f0c99
Source noteuspto-grants-2013_01