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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283906Generated: October 31, 2026

Indole → Ethyl 3-indolylglyoxylate

https://huagongshe.com/reaction/2283906

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.) solution 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 numberUS09145410B2
Source datasetuspto-grants-2015_09
ORD IDord-61d944f69d374403a2e6265be4a87a48
Source noteuspto-grants-2015_09