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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095346Generated: October 25, 2026

Indole → Ethyl 3-indolylglyoxylate

https://huagongshe.com/reaction/1095346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantPyridineHCID 1049—
ReactantEthoxalyl chlorideHCID 20884—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-indolylglyoxylateHCID 10124284.2%

Reaction Steps

Pyridine (40 mL, 492 mmol) was added in a single portion to a chilled solution (0° C.) of indole (48 g, 410 mmol) in diethyl ether (820 mL). Ethyl chlorooxoacetate (50 mL, 451 mmol) was added dropwise. The resulting suspension was allowed to warm to ambient temperature over a period of 20 hours. The solid was isolated by filtration and washed with diethyl ether. The solid was combined with water (1 L), stirred for 1 hour, and then isolated by filtration to provide 75 g of ethyl (1H-indol-3-yl)(oxo)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138173B2
Source datasetuspto-grants-2012_03
ORD IDord-e538b1bf3a20418aa517a7cf341d7ab0
Source noteuspto-grants-2012_03