Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590977Generated: October 26, 2026

Ethoxalyl chloride → ethyl (1-methyl-2-phenyl-1H-indol-3-yl)-oxo-acetate

https://huagongshe.com/reaction/590977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
Reactant1-Methyl-2-phenylindoleHCID 77095—
ReactantSodium BicarbonateHCID 516892—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Productethyl (1-methyl-2-phenyl-1H-indol-3-yl)-oxo-acetateHCID 7085525343%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., aluminum (III) chloride (2.5 g, 19 mmol) was added per portion to a solution of 1-methyl-2-phenyl-1H-indole (1 g, 4.8 mmol) and ethyl chlorooxoacetate (900 μL, 8.05 mmol) in dichloromethane (10 mL). The mixture was stirred for 2 hours at 0° C. and then hydrolyzed with a saturated solution of sodium bicarbonate. After removing the aqueous layer, organic layer was washed with water, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to afford the desired keto-ester (8a) (630 mg, 2.05 mmol, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-866331b423cb4203b3edccc029b13bb9
Source noteuspto-grants-2016_01