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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034072Generated: October 27, 2026

Indole → 5-Nitrofuroyl chloride

https://huagongshe.com/reaction/1034072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant5-Nitro-2-Furoic AcidHCID 12577—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product5-Nitrofuroyl chlorideHCID 90711—
Product3-(5-Nitro-2-furoyl)indoleHCID 19024851—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 5-nitro-2-furoyl chloride, which was prepared with 5-nitro-2-furoic acid (2.0 g) and oxalyl chloride (1.4 ml) in an usual manner, in dichloromethane (10 ml) was added to a suspension at aluminum chloride (1.78 g) at 25° C. The mixture was stirred at 25° C. for 30 minutes, and then a solution of indole (1.49 g) in dichloromethane (15 ml) was added at 25° C. The mixture was stirred at 25° C. for 1 hour, and poured into ice water. The precipitates were filtered and washed with water, ethyl acetate and hot ethanol to give 3-(5-nitro-2-furoyl)indole (1.08 g) as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312829
Source datasetuspto-grants-1994_05
ORD IDord-5eb4a5c3f3cc4cc5a299cc314d755c64
Source noteuspto-grants-1994_05