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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017587Generated: October 30, 2026

Water → 2-(1-Methyl-1H-indol-3-YL)-2-oxoacetic acid methyl ester

https://huagongshe.com/reaction/1017587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylindoleHCID 11781—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium MethoxideHCID 10942334—
SolventDiethyl EtherHCID 3283—
Product2-(1-Methyl-1H-indol-3-YL)-2-oxoacetic acid methyl esterHCID 445367582.8%

Reaction Conditions

Temperature-65 °C

Reaction Steps

To a 0° C. solution of 1-methylindole (7.58 g, 50 mmoles) in dry ether (75 mL) under argon was added oxalyl chloride (4.36 mL, 50 mmoles) slowly. The resulting suspension was stirred for 30 minutes. After cooling to −65° C, sodium methoxide (22.9 mL, 100 mmoles, 25% in MeOH) was added dropwise at a rate to maintain −60° C. After the addition was complete, the reaction was allowed to warm to room temperature and stir for 2 hours. Water was added (30 mL) and the crude mixture was stirred then filtered. The resultant solid was washed with water, ether and then air dried. Purification of the crude product via flash chromatography (SiO2, 20% to 40% ethyl acetate/Hexane—gradient) provided methyl (1-methyl-1H-indol-3-yl)(oxo)acetate as a solid (9 g, 41.4 mmoles).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479490B2
Source datasetuspto-grants-2002_11
ORD IDord-c499bff7f78f4fd4880487ae88a57099
Source noteuspto-grants-2002_11