HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825747Generated: October 25, 2026
Dimethylformamide → Methyl 3-formyl-1H-indole-7-carboxylate
https://huagongshe.com/reaction/1825747
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Methyl indole-7-carboxylate | HCID 676694 | — |
| Reactant | DMF Phosphorus oxychloride | HCID 13765457 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Methyl 3-formyl-1H-indole-7-carboxylate | HCID 762965 | 93% |
Reaction Steps
To a stirred mixture of phosphorus oxychloride-dimethylformamide in anhydrous 1,2-dichloroethane (prepared by the slow addition of phosphorus oxychloride (0.43 ml, 4.6 mmol) to anhydrous DMF (0.35 ml, 4.6 mmol) in anhydrous 1,2-dichloroethane (6 ml) cooled below 5° C.) a solution of 7-methoxycarbonylindole (0.69 g, 4 mmol) in anhydrous 1,2-dichloroethane (6 ml) was dropwise below 5° C. The mixture was stirred at room temperature for 2 h and then was heated at 50° C. for 30 minutes. After cooling, the precipitate was filtered off and washed with 1,2-dichloroethane. This precipitate was suspended in aq Na2CO3 10% (30 ml) and stirred at room temperature for 20 minutes; dichloromethane was added and stirring was continued 10 minutes more. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate and evaporated to yield 0.75 g (93%) of the entitled product. Mp: 153–4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07049312B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-1b6c9aa600274133865828d9e9ab2640 |
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| Source note | uspto-grants-2006_05 |
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