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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantMethyl indole-7-carboxylateHCID 676694—
ReactantDMF Phosphorus oxychlorideHCID 13765457—
Solvent1,2-DichloroethaneHCID 11—
ProductMethyl 3-formyl-1H-indole-7-carboxylateHCID 76296593%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049312B1
Source datasetuspto-grants-2006_05
ORD IDord-1b6c9aa600274133865828d9e9ab2640
Source noteuspto-grants-2006_05