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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338278Generated: October 25, 2026

Water → 5-Bromo-4,6-difluoro-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/338278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantN-(Chloromethylidene)-N-methylmethanaminiumHCID 77312—
Reactant5-bromo-4,6-difluoro-1H-indoleHCID 68054999—
SolventDimethylformamideHCID 6228—
Product5-Bromo-4,6-difluoro-1H-indole-3-carbaldehydeHCID 86698578—

Reaction Steps

To a solution of 5-bromo-4,6-difluoro-1H-indole (285 mg, 1.23 mmol) in DMF (2 mL) was added N-(chloromethylidene)-N-methylmethanaminium (236 mg, 1.84 mmol) at room temperature. The reaction mixture was stirred for 30 min, and treated with additional N-(chloromethylidene)-N-methylmethanaminium (100 mg). The mixture was stirred for an additional 30 minutes at room temperature. The reaction mixture was then treated with 1N aqueous NaOH (2.5 mL) and water (2.5 mL). The mixture was stirred at 100° C. for 30 min. After cooling to room temperature, the solvents were evaporated in vacuo, and the residue was diluted with THF (2 mL) and water (2 mL). The resulting mixture was stirred at room temperature for 2 hours, and the resulting solids were collected by filtration. The solids were washed with water and heptanes and dried in vacuo to give the title compound (157 mg) as a brown solid. MS (ES+) 261.8 ((M+2)+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-94877df172134b3e9045a301bcdf3b08
Source noteuspto-grants-2014_11