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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054621Generated: October 27, 2026

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

https://huagongshe.com/reaction/1054621

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 1 N 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 numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-df0cc8852dbd41a3a543556a0a7fb273
Source noteuspto-grants-2016_07