HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642047Generated: October 31, 2026
Dimethylformamide → 6-Chloro-1H-indole-3-carboxaldehyde
https://huagongshe.com/reaction/1642047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Chloroindole | HCID 87111 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Chloro-1H-indole-3-carboxaldehyde | HCID 12614669 | 88% |
Reaction Steps
This Vilsmeyer reaction was performed according to H. G. O. Becker, Organikum, pp. 364-365, Johann Ambrosius Barth Verlag, Heidelberg-Leipzig (1996). To 5 mL DMF in a three-necked flask equipped with a thermometer, 1.8 mL POCl3 was added dropwise in a temperature range between 15° C. and 20° C. Then, a solution of 1 g (6.6 mMol) of 6-chloro-1H-indole in 2 mL DMF was added dropwise in a temperature range between 20° C. and 30° C. The reaction mixture was stirred for 45 minutes at 37° C. Afterwards, the reaction mixture was poured in a mixture of 15 g ice in 10 mL water under stirring. 3.4 g NaOH in 18 mL were added between in a temperature range between 20 and 30° C. The resulting mixture was then refluxed for 5 minutes. After cooling to room temperature, the precipitate was filtered off and washed with 10 mL cold water. Crystallization from ethanol yielded 6-chloro-1H-indole-3-carbaldehyde as a white solid (1.04 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119623B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-ca9b2d26d5094cac9f878a78dbdd228a |
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| Source note | uspto-grants-2012_02 |
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