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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651763Generated: October 25, 2026

Methyl chloroglyoxylate → methyl (1-methyl-6-morpholin-4-yl-1H-indol-3-yl)glyoxylate

https://huagongshe.com/reaction/651763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroglyoxylateHCID 79846—
Reactant1-methyl-6-morpholin-4-yl-1H-indoleHCID 21709060—
SolventDichloromethaneHCID 6344—
Productmethyl (1-methyl-6-morpholin-4-yl-1H-indol-3-yl)glyoxylateHCID 86757285110.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Methyl-6-morpholin-4-yl-1H-indole (3.89 g, 18 mmol) was dissolved in CH2Cl2 (18 mL) and cooled at 0° C. Methyl chlorooxoacetate (2.4 mL, 26 mmol) was added to give a dark solution. Stirring was continued for 2 h at 0° C. and more methyl chlorooxoacetate (0.40 mL, 4.3 mmol) was added. After a further 2 h, the solvent was evaporated. The resulting solid was taken up in ether, filtered and washed well with ether to give crude methyl (1-methyl-6-morpholin-4-yl-1H-indol-3-yl)glyoxylate (6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281356B1
Source datasetuspto-grants-2001_08
ORD IDord-0a0cc69973674b51a6d140f6456c249d
Source noteuspto-grants-2001_08