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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070694Generated: October 30, 2026

(5,6-dichloro-1H-indol-2-yl)methanol → 5,6-dichloro-1H-indole-2-carbaldehyde

https://huagongshe.com/reaction/1070694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5,6-dichloro-1H-indol-2-yl)methanolHCID 22397554—
CatalystManganese dioxideHCID 14801—
SolventDiethyl EtherHCID 3283—
Product5,6-dichloro-1H-indole-2-carbaldehydeHCID 1084627790.5%

Reaction Steps

A solution of 5,6-dichloroindole-2-methanol (43 g, 199 mmol) in diethyl ether (1.3 l) was treated with activated MnO2 (64 g, 730 mmol) and stirred for 15 hours at room temperature. Additional MnO2 (20 g, 230 mmol) was added and stirring continued for 5 h. The suspension was filtered on a Celite pad, then the pad was washed with diethyl ether and warm acetone. The pooled organic phases were concentrated to give 38.5 g of the title compound (180 mmol, yield 90.4%) that was used as such in the next step, m.p.=207-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903117B2
Source datasetuspto-grants-2005_06
ORD IDord-d541b3ef956e44dcb99d55482b61dea7
Source noteuspto-grants-2005_06