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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749736Generated: October 26, 2026

1,2-Dichloroethane → 5-(2-morpholinoethoxy)-1H-indole-3-carboxaldehyde

https://huagongshe.com/reaction/1749736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-[2-(1H-indol-5-yloxy)ethyl]morpholineHCID 22135442—
SolventDimethylformamideHCID 6228—
Product5-(2-morpholinoethoxy)-1H-indole-3-carboxaldehydeHCID 8668193250%

Reaction Steps

Under an argon atmosphere, a solution of 4-[2-(1H-indol-5-yloxy)ethyl]morpholine (0.12 g, 0.5 mmol) in 1,2-dichloroethane (2.0 mL) was added dropwise with a solution of phosphorus oxychloride (0.1 mL) and N,N-dimethylformamide (0.1 mL) in 1,2-dichloroethane (1.0 mL). The mixture was stirred at room temperature for 1 hour, and then added with 3 N aqueous potassium hydroxide, and the mixture was stirred at 60° C. for 2 hours. The aqueous layer was adjusted to pH 7 with 3 N hydrochloric acid, and then extracted with ethyl acetate. The resulting organic layer was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the residue was suspended in a mixed solvent of ethyl acetate and hexane and thereby washed to obtain 5-(2-morpholinoethoxy)-1H-indole-3-carboxaldehyde (0.068 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-f26ea1b158154daf8e01618c78fd3285
Source noteuspto-grants-2015_10