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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720329Generated: November 1, 2026

5-(4-Chlorobenzyl)-4-methoxymethyl-beta-carboline-3-methanol → 5-(4-Chlorobenzyl)-4-methoxymethyl-beta-carboline-3-carbaldehyde

https://huagongshe.com/reaction/1720329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Chlorobenzyl)-4-methoxymethyl-beta-carboline-3-methanolHCID 22417750—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product5-(4-Chlorobenzyl)-4-methoxymethyl-beta-carboline-3-carbaldehydeHCID 2241772774.3%

Reaction Steps

1.3 g (0.00354 mol) of 5-(4-chlorobenzyl)-4-methoxymethyl-β-carboline-3-methanol is stirred for 192 hours under argon at room temperature with 1.74 g (0.02 mol) of manganese dioxide in 200 ml of dichloromethane. The manganese dioxide is suctioned off, the filtrate concentrated by evaporation and the residue recrystallized from ethanol. Thus 0.96 g (74% of theory) of 5-(4-chlorobenzyl)-4-methoxymethyl-β-carboline-3-carbaldehyde is obtained, melting point 248°-250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506234
Source datasetuspto-grants-1996_04
ORD IDord-ba4498f838774ca18d0b577d1f4c0acd
Source noteuspto-grants-1996_04