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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657312Generated: November 2, 2026

Pyridine → 3-Methyl-1-(phenylsulfonyl)-2-indoleacetaldehyde

https://huagongshe.com/reaction/1657312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-[3-Methyl-1-(phenylsulfonyl)indol-2-yl]ethanolHCID 10313611—
Catalystchromium (VI) trioxideHCID 10219390—
SolventDichloromethaneHCID 6344—
Product3-Methyl-1-(phenylsulfonyl)-2-indoleacetaldehydeHCID 1042572767.6%

Reaction Steps

A mixture of chromium trioxide (1.2 g) and pyridine (1.9 g) in dichloromethane was stirred at ambient temperature for 15 minutes, and then 2-[3-methyl-1-(phenylsulfonyl)indol-2-yl]ethanol (630 mg) in dichloromethane [2 ml) was added. The resultant mixture was stirred at room temperature for 15 minutes. The separated organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed over silica gel (eluted with 5% ethyl acetate in toluene) to give 3-methyl-1-(phenylsulfonyl)-2-indole acetaldehyde (423 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256780
Source datasetuspto-grants-1993_10
ORD IDord-90c6748ba12647b685a6c533de62c0c9
Source noteuspto-grants-1993_10