HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485335Generated: October 30, 2026
Dimethylformamide → HCID 13490349, compound
https://huagongshe.com/reaction/485335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1-(pyridin-3-yl)-1H-indole | HCID 13490348 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13490349 | HCID 13490349 | — |
Reaction Steps
A solution of 2.12 ml of N,N-dimethylformamide in 20 ml of 1,2-dichloroethane is cooled to 0° and 3.1 ml of phosphorus oxychloride is added dropwise. The reaction is stirred for 10 minutes at 15° and recooled to 0° before a solution of 4.85 g of N-(3-pyridyl)indole in 10 ml of 1,2-dichloroethane is added. After 2 hours at 5°, the reaction mixture is refluxed for 15 minutes, cooled to room temperature and a solution of 18.75 g of sodium acetate trihydrate in 25 ml of water is added. After an additional 15 minutes at reflux, the organic phase is separated, washed with sodium bicarbonate and water, and dried over magnesium sulfate. Filtration, evaporation and recrystallization of the residue from methylene chloride-methanol yields N-(3-pyridyl)-indole-3-carboxaldehyde, m.p. 148°-150°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536505 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-e322f9da7d7d4ac1b4a8eb482f2c1432 |
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| Source note | uspto-grants-1985_08 |
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