HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250199Generated: October 25, 2026
Dimethylformamide → 4-Methoxyindole-3-aldehyde
https://huagongshe.com/reaction/250199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-Methoxy-1H-indole | HCID 138363 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-Methoxyindole-3-aldehyde | HCID 146229 | 96.3% |
Reaction Steps
A solution of dry DMF (0.75 g) in 50 ml dichloroethane was cooled to 0° C. and placed under nitrogen. Oxalyl chloride (1.03 g) dissolved in dichloroethane (5 ml) was added dropwise with stirring. The solution was stirred until no more bubbling was observed (about 15-20 m). 4-Methoxyindole (1.0 g, 6.7 mmole) was added to the solution as a solid and the reaction mixture was stirred at room temperature for four hours. The reaction was quenched by careful addition of 10% sodium carbonate solution. The two phase mixture was stirred at room temperature for 2 hours. The layers were separated and the aqueous layer was extracted with methylene chloride, and the combined organic extracts were dried and evaporated to dryness. The crude residue was passed through a short silica gel column, eluting with 3:7 ethyl acetate:hexane to 1:1 ethyl acetate:hexane to yield 1.13 g (95%) of 4-methoxy-1H-indole-3-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07863305B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-49570dac9afd4c6fa553e2c3fbddfdf1 |
|---|
| Source note | uspto-grants-2011_01 |
|---|