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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371656Generated: October 31, 2026

Diethyl Oxalate → HCID 12620579, compound

https://huagongshe.com/reaction/371656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant1-(3-hydroxy-1-methyl-1H-indol-2-yl)ethanoneHCID 4712191—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 12620579HCID 12620579—

Reaction Steps

To a solution of 6.0g (0.26 mole) of sodium metal in 600ml ab. ethanol was added to 18.0g (0.095 mole) of 3-hydroxy-1-methyl-1H-indol-2-yl methyl ketone, followed by 37.6g (0.26 mole) of diethyl oxalate, added over 10 min. The mixture was stirred and heated at reflux for 17 hours, cooled and the red di-sodium salt was filtered and washed with cold hexane. The crude salt was added to a solution of 28ml conc. HCl and 120ml ab. ethanol, heated at reflux for 30 min., and the mixture was filtered while hot. Cooling the filtrate gave the crude product, which was filtered and then dissolved in 400ml of chloroform. The chloroform solution was washed 3 times with dilute aqueous NaHCO3, 1 time with water, dried (MgSO4) and evaporated to leave a grey residue. Recrystallization from 15% CHCl3 in hexane gave yellow needles of mpt. 160°-162°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087443
Source datasetuspto-grants-1978_05
ORD IDord-707b3b86900046de81c6fdbc07b0d956
Source noteuspto-grants-1978_05