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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-[2-(1H-indol-5-yloxy)ethyl]morpholine | HCID 22135442 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-morpholinoethoxy)-1H-indole-3-carboxaldehyde | HCID 86681932 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09156827B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-f26ea1b158154daf8e01618c78fd3285 |
|---|
| Source note | uspto-grants-2015_10 |
|---|