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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488868Generated: November 3, 2026

5-Methoxytryptamine → Melatonin

https://huagongshe.com/reaction/1488868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-MethoxytryptamineHCID 1833—
ReactantAcetic AnhydrideHCID 7918—
SolventDichloromethaneHCID 6344—
ProductMelatoninHCID 8960.1%

Reaction Steps

To a suspension, cooled in ice, of 5 g (26.3 moles) of 5-methoxytryptamine (in a raw condition) in 100 ml methylene chloride there is slowly added, under stirring, a cold solution of 5 ml (52.6 moles) of acetic anhydride in 50 ml of methylene chloride. Stirring and cooling are continued for 1 hour (the reaction progression can be controlled by TLC), so as to obtain a .[.full.]. complete solution; then the solution is washed by Na2CO3 2N×2, under strong stirring, and then by water. The organic phase, dried on anhydrous Na2SO4 and evaporated, provides 6 g of .[.raw melatonine,.]. crude melatonin which is purified by chromatography on column (4 cm; diameter/length ratio 1:5) of Merck silica gel (70-230 mesh) (120 g); the solution is eluted by methylene chloride in order to remove the scarcely polar products thereby providing pure .[.melatonine.]. melatonin by eluting with methylene chloride-acetone (8.2). There are obtained 4 g of product (purifying yield 65%) which are .[.crystalized.]. crystallized from acetone-water. Melting point 116°-7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE035631
Source datasetuspto-grants-1997_10
ORD IDord-5027044bc2a2471b97815439d5db3283
Source noteuspto-grants-1997_10