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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845233Generated: October 30, 2026

Potassium Carbonate → 5-Acetoxymethyl-4-methoxymethyl-1,2,3,4-tetrahydro-beta-carboline-1,3-dicarboxylic acid-3 ethyl ester

https://huagongshe.com/reaction/845233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
Reactant3-(4-Acetoxymethylindol-3-yl)-2-amino-4-methoxy-butyric acid ethyl esterHCID 53929152—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-Acetoxymethyl-4-methoxymethyl-1,2,3,4-tetrahydro-beta-carboline-1,3-dicarboxylic acid-3 ethyl esterHCID 20132390—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-(4-acetoxymethylindol-3-yl)-2-amino-4-methoxy-butyric acid ethyl ester (8.7 g) in ethyl acetate (40 ml) is slowly added drop by drop to a solution of glyoxylic acid monohydrate (2.4 g) in water (30 ml), cooled to 0° C., under argon protection and with stirring. The pH of the solution is adjusted to 4 by addition of potassium carbonate (about 1 g). Then the mixture is stirred for 2 hours, whereby it is allowed to warm to room temperature. Ethyl acetate and water phases are separated, the water phase is shaken out three times with ethyl acetate. The combined ethyl acetate extracts, for their part, are washed once with water, dried with sodium sulfate and evaporated. 9 g of the title compound remains.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04757070
Source datasetuspto-grants-1988_07
ORD IDord-fb09866dd06c442a8b4d97e101b92b5f
Source noteuspto-grants-1988_07