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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338446Generated: October 29, 2026

Dimethylformamide → 6-Chloro-5-(4-(2-hydroxyethyl)-3-methoxyphenyl)-1h-indole-3-carbaldehyde

https://huagongshe.com/reaction/338446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantChloro-N,N-dimethylformiminium chlorideHCID 77311—
Reactant2-(4-Bromo-2-methoxyphenyl)ethanolHCID 66580015—
Reactant6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indoleHCID 86698733—
Product6-Chloro-5-(4-(2-hydroxyethyl)-3-methoxyphenyl)-1h-indole-3-carbaldehydeHCID 86698777—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a 0.4M solution of chlormethylene dimethylammonium chloride in DMF (7.5 mL, 3.8 mmol) was added 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (493 mg, 1.88 mmol). The mixture was stirred at 30° C. for 2 hrs. 0.50 mL of this solution (0.15 mmol) was placed in a vial with a 0.3M solution of 2-(4-bromo-2-methoxyphenyl)ethanol in DMF (0.50 mL, 0.15 mmol). 2M potassium carbonate (0.30 mL, 0.60 mmol) was then added and the mixture was purged with nitrogen. PddppfCl2 (9 mg, 0.01 mmol) was then added and the vial capped and heated to 90° C. for 3 hours. The reaction mixture was concentrated by Speedvac and purified via preparative TLC to give the title compound that was taken forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-7ca502a1c01a4f7a9dbad1828c355557
Source noteuspto-grants-2014_11