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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630754Generated: October 30, 2026

HCID 58443296, compound → HCID 58443257, compound

https://huagongshe.com/reaction/1630754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58443296HCID 58443296—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
ProductHCID 58443257HCID 58443257—

Reaction Steps

To a solution of (9-ethyl-9H-β-carbolin-3-yl)-methanol (560 mg, 2.47 mmol, 1 eq) in acetone (20 mL) was added manganese (IV) oxide (2.942 g, 33.84 mmol, 14 eq). The solution was stirred at rt. After 3 d, as only 50% conversion is observed, more manganese (IV) oxide was added (229 mg, 2.63 mmol, 1.1 eq) and the mixture was heated to 50° C. for 2.5 d. After this time, the reaction was cooled down to rt, filtered through CELITE®, and the solid was washed with dichloromethane. The filtrates were combined and concentrated under reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate to give the title compound as a yellow oil. Mass Spec m/z=225 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791147B2
Source datasetuspto-grants-2014_07
ORD IDord-198bf40d1c804e0eb1a5cc9b78c0f747
Source noteuspto-grants-2014_07