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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206601Generated: October 31, 2026

Trichloroacetyl chloride → 2,2,2-trichloro-1-(2-methyl-1H-pyrrolo[2,3-c]pyridin-3-yl)ethanone

https://huagongshe.com/reaction/2206601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Methyl-1H-pyrrolo(2,3-c)pyridineHCID 12407505—
SolventDichloromethaneHCID 6344—
Product2,2,2-trichloro-1-(2-methyl-1H-pyrrolo[2,3-c]pyridin-3-yl)ethanoneHCID 117778940100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-methyl-1H-pyrrolo[2,3-c]pyridine (2.5 g, 18.9 mmol) and aluminum chloride (5 g, 37.8 mmol) in DCM (100 mL), trichloroacetylchloride (4.1 g, 22.7 mmol) was added dropwise into the reaction over 0.5 hours at room temperature. After stirring 2 hours, the reaction was cooled to 0° C. and was quenched with water (100 mL). The resulting precipitate was isolated by filtration to afford 2,2,2-trichloro-1-(2-methyl-1H-pyrrolo[2,3-c]pyridin-3-yl)ethanone which was used for next step without further purification. Assumed 100% yield. (5.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-960f529993c048bc81a8e9c1df1238e8
Source noteuspto-grants-2016_06